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dbVar

Database of genomic structural variation

esv3689116

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: 394 SVs from 35 studies. See in: genome view

Remapped(Score: Perfect):1,176,636-1,176,636

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3689116	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000008.11	Chr8	1,176,636	1,176,636
esv3689116	Remapped	Perfect	GRCh38.p12	ALT_REF_LOCI_2	Second Pass	NT_187655.1	Chr8\|NT_18 7655.1	35,190	35,190
esv3689116	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000008.10	Chr8	1,126,636	1,126,636

Variant Call Information

Variant Call ID	Type	Method	Analysis
essv16473282	insertion	Sequencing	de novo sequence assembly

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv16473282	Remapped	Perfect	NT_187655.1:g.3519 0_35191ins58	GRCh38.p12	Second Pass	NT_187655.1	Chr8\|NT_18 7655.1	35,190	35,190
essv16473282	Remapped	Perfect	NC_000008.11:g.117 6636_1176637ins58	GRCh38.p12	First Pass	NC_000008.11	Chr8	1,176,636	1,176,636
essv16473282	Submitted genomic		NC_000008.10:g.112 6636_1126637ins58	GRCh37 (hg19)		NC_000008.10	Chr8	1,126,636	1,126,636

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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