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dbVar

Database of genomic structural variation

esv1914953

Organism: Homo sapiens

Study:estd193 (Feuk et al. 2005)
Variant Type:inversion
Method Type:PCR
Submitted on:NCBI35 (hg17)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:17,918

Publication(s):Feuk et al. 2005

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: 454 SVs from 78 studies. See in: genome view

Remapped(Score: Perfect):70,955,984-70,973,901

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv1914953	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000007.14	Chr7	70,955,984	70,973,901
esv1914953	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	70,420,970	70,438,887
esv1914953	Submitted genomic		NCBI35 (hg17)	Primary Assembly		NC_000007.11	Chr7	69,865,621	69,883,538

Variant Call Information

Variant Call ID	Type	Method	Analysis
essv4491060	inversion	PCR	Manual observation

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv4491060	Remapped	Perfect	NC_000007.14:g.709 55984_70973901inv	GRCh38.p12	First Pass	NC_000007.14	Chr7	70,955,984	70,973,901
essv4491060	Remapped	Perfect	NC_000007.13:g.704 20970_70438887inv	GRCh37.p13	First Pass	NC_000007.13	Chr7	70,420,970	70,438,887
essv4491060	Submitted genomic		NC_000007.11:g.698 65621_69883538inv	NCBI35 (hg17)		NC_000007.11	Chr7	69,865,621	69,883,538

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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