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dbVar

Database of genomic structural variation

nsv426187

Organism: Homo sapiens

Study:nstd6 (Mills et al. 2006)
Variant Type:insertion
Method Type:Sequencing
Submitted on:NCBI35 (hg17)

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

Publication(s):Mills et al. 2006

Links to Other Resources

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: 342 SVs from 18 studies. See in: genome view

Remapped(Score: Perfect):10,068,929-10,068,929

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv426187	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000024.10	ChrY	10,068,929	10,068,929
nsv426187	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000024.9	ChrY	9,906,538	9,906,538
nsv426187	Submitted genomic		NCBI35 (hg17)	Primary Assembly		NC_000024.7	ChrY	10,499,899	10,499,899

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv444765	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv444765	Remapped	Perfect	NC_000024.10:g.100 68929_10068930insC CACCTCCACCT	GRCh38.p12	First Pass	NC_000024.10	ChrY	10,068,929	10,068,929
nssv444765	Remapped	Perfect	NC_000024.9:g.9906 538_9906539insCCAC CTCCACCT	GRCh37.p13	First Pass	NC_000024.9	ChrY	9,906,538	9,906,538
nssv444765	Submitted genomic		NC_000024.7:g.1049 9899_10499900insCC ACCTCCACCT	NCBI35 (hg17)		NC_000024.7	ChrY	10,499,899	10,499,899

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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