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dbVar

Database of genomic structural variation

esv3689128

Organism: Homo sapiens

Study:estd217 (Besenbacher et al. 2015)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh37 (hg19)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1

Publication(s):Besenbacher et al. 2015

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 350 SVs from 39 studies. See in: genome view

Remapped(Score: Perfect):1,521,460-1,521,460

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3689128	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000008.11	Chr8	1,521,460	1,521,460
esv3689128	Remapped	Perfect	GRCh38.p12	ALT_REF_LOCI_1	Second Pass	NT_187565.1	Chr8\|NT_18 7565.1	226,992	226,992
esv3689128	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000008.10	Chr8	1,469,626	1,469,626

Variant Call Information

Variant Call ID	Type	Method	Analysis
essv16473293	insertion	Sequencing	de novo sequence assembly

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv16473293	Remapped	Perfect	NT_187565.1:g.2269 92_226993ins56	GRCh38.p12	Second Pass	NT_187565.1	Chr8\|NT_18 7565.1	226,992	226,992
essv16473293	Remapped	Perfect	NC_000008.11:g.152 1460_1521461ins56	GRCh38.p12	First Pass	NC_000008.11	Chr8	1,521,460	1,521,460
essv16473293	Submitted genomic		NC_000008.10:g.146 9626_1469627ins56	GRCh37 (hg19)		NC_000008.10	Chr8	1,469,626	1,469,626

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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