Warning: The NCBI web site requires JavaScript to function. more...

dbVar

Database of genomic structural variation

esv3689121

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: 382 SVs from 34 studies. See in: genome view

Remapped(Score: Perfect):1,318,843-1,318,843

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3689121	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000008.11	Chr8	1,318,843	1,318,843
esv3689121	Remapped	Perfect	GRCh38.p12	ALT_REF_LOCI_1	Second Pass	NT_187565.1	Chr8\|NT_18 7565.1	38,059	38,059
esv3689121	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000008.10	Chr8	1,267,009	1,267,009

Variant Call Information

Variant Call ID	Type	Method	Analysis
essv16473287	insertion	Sequencing	de novo sequence assembly

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv16473287	Remapped	Perfect	NT_187565.1:g.3805 9_38060ins262	GRCh38.p12	Second Pass	NT_187565.1	Chr8\|NT_18 7565.1	38,059	38,059
essv16473287	Remapped	Perfect	NC_000008.11:g.131 8843_1318844ins262	GRCh38.p12	First Pass	NC_000008.11	Chr8	1,318,843	1,318,843
essv16473287	Submitted genomic		NC_000008.10:g.126 7009_1267010ins262	GRCh37 (hg19)		NC_000008.10	Chr8	1,267,009	1,267,009

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

You are here: NCBI