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dbVar

Database of genomic structural variation

esv3666922

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:63

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: 110 SVs from 23 studies. See in: genome view

Remapped(Score: Perfect):83,060,050-83,060,112

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3666922	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000005.10	Chr5	83,060,050	83,060,112
esv3666922	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000005.9	Chr5	82,355,869	82,355,931

Variant Call Information

Variant Call ID	Type	Method	Analysis
essv16489433	inversion	Sequencing	de novo sequence assembly

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv16489433	Remapped	Perfect	NC_000005.10:g.830 60050_83060112inv6 2	GRCh38.p12	First Pass	NC_000005.10	Chr5	83,060,050	83,060,112
essv16489433	Submitted genomic		NC_000005.9:g.8235 5869_82355931inv62	GRCh37 (hg19)		NC_000005.9	Chr5	82,355,869	82,355,931

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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