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dbVar

Database of genomic structural variation

esv3689107

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: 352 SVs from 36 studies. See in: genome view

Remapped(Score: Perfect):999,480-999,480

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3689107	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000008.11	Chr8	999,480	999,480
esv3689107	Remapped	Perfect	GRCh38.p12	ALT_REF_LOCI_1	Second Pass	NT_187568.1	Chr8\|NT_18 7568.1	140,770	140,770
esv3689107	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000008.10	Chr8	949,480	949,480

Variant Call Information

Variant Call ID	Type	Method	Analysis
essv16473274	insertion	Sequencing	de novo sequence assembly

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv16473274	Remapped	Perfect	NT_187568.1:g.1407 70_140771ins59	GRCh38.p12	Second Pass	NT_187568.1	Chr8\|NT_18 7568.1	140,770	140,770
essv16473274	Remapped	Perfect	NC_000008.11:g.999 480_999481ins59	GRCh38.p12	First Pass	NC_000008.11	Chr8	999,480	999,480
essv16473274	Submitted genomic		NC_000008.10:g.949 480_949481ins59	GRCh37 (hg19)		NC_000008.10	Chr8	949,480	949,480

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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