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dbVar

Database of genomic structural variation

esv3671450

Organism: Homo sapiens

Study:estd217 (Besenbacher et al. 2015)
Variant Type:novel sequence 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: 130 SVs from 27 studies. See in: genome view

Remapped(Score: Perfect):145,892,670-145,892,670

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3671450	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000004.12	Chr4	145,892,670	145,892,670
esv3671450	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000004.11	Chr4	146,813,822	146,813,822

Variant Call Information

Variant Call ID	Type	Method	Analysis
essv16493508	novel sequence insertion	Sequencing	de novo sequence assembly

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv16493508	Remapped	Perfect	NC_000004.12:g.145 892670_145892671in s319	GRCh38.p12	First Pass	NC_000004.12	Chr4	145,892,670	145,892,670
essv16493508	Submitted genomic		NC_000004.11:g.146 813822_146813823in s319	GRCh37 (hg19)		NC_000004.11	Chr4	146,813,822	146,813,822

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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