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dbVar

Database of genomic structural variation

esv3666929

Organism: Homo sapiens

Study:estd217 (Besenbacher et al. 2015)
Variant Type:inversion
Method Type:Sequencing
Submitted on:GRCh37 (hg19)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:360

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: 151 SVs from 37 studies. See in: genome view

Remapped(Score: Perfect):105,054,356-105,054,715

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3666929	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000009.12	Chr9	105,054,356	105,054,715
esv3666929	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000009.11	Chr9	107,816,637	107,816,996

Variant Call Information

Variant Call ID	Type	Method	Analysis
essv16489440	inversion	Sequencing	de novo sequence assembly

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv16489440	Remapped	Perfect	NC_000009.12:g.105 054356_105054715in v343	GRCh38.p12	First Pass	NC_000009.12	Chr9	105,054,356	105,054,715
essv16489440	Submitted genomic		NC_000009.11:g.107 816637_107816996in v343	GRCh37 (hg19)		NC_000009.11	Chr9	107,816,637	107,816,996

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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