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dbVar

Database of genomic structural variation

esv3666945

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:245

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

Remapped(Score: Perfect):13,997,427-13,997,671

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3666945	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000018.10	Chr18	13,997,427	13,997,671
esv3666945	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000018.9	Chr18	13,997,426	13,997,670

Variant Call Information

Variant Call ID	Type	Method	Analysis
essv16489454	inversion	Sequencing	de novo sequence assembly

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv16489454	Remapped	Perfect	NC_000018.10:g.139 97427_13997671inv2 44	GRCh38.p12	First Pass	NC_000018.10	Chr18	13,997,427	13,997,671
essv16489454	Submitted genomic		NC_000018.9:g.1399 7426_13997670inv24 4	GRCh37 (hg19)		NC_000018.9	Chr18	13,997,426	13,997,670

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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