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dbVar

Database of genomic structural variation

esv3666944

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:95

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: 184 SVs from 31 studies. See in: genome view

Remapped(Score: Perfect):80,763,242-80,763,336

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3666944	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000016.10	Chr16	80,763,242	80,763,336
esv3666944	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000016.9	Chr16	80,797,139	80,797,233

Variant Call Information

Variant Call ID	Type	Method	Analysis
essv16489453	inversion	Sequencing	de novo sequence assembly

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv16489453	Remapped	Perfect	NC_000016.10:g.807 63242_80763336inv9 4	GRCh38.p12	First Pass	NC_000016.10	Chr16	80,763,242	80,763,336
essv16489453	Submitted genomic		NC_000016.9:g.8079 7139_80797233inv94	GRCh37 (hg19)		NC_000016.9	Chr16	80,797,139	80,797,233

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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