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dbVar

Database of genomic structural variation

esv3671460

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: 134 SVs from 26 studies. See in: genome view

Remapped(Score: Perfect):150,276,960-150,276,960

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3671460	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000004.12	Chr4	150,276,960	150,276,960
esv3671460	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000004.11	Chr4	151,198,112	151,198,112

Variant Call Information

Variant Call ID	Type	Method	Analysis
essv16493517	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
essv16493517	Remapped	Perfect	NC_000004.12:g.150 276960_150276961in s207	GRCh38.p12	First Pass	NC_000004.12	Chr4	150,276,960	150,276,960
essv16493517	Submitted genomic		NC_000004.11:g.151 198112_151198113in s207	GRCh37 (hg19)		NC_000004.11	Chr4	151,198,112	151,198,112

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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