Warning: The NCBI web site requires JavaScript to function. more...

dbVar

Database of genomic structural variation

nsv475165

Organism: Homo sapiens

Study:nstd35 (Kidd et al. 2010)
Variant Type:complex substitution
Method Type:Sequencing
Submitted on:NCBI36 (hg18)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:5

Description:complex allele - no allele length provided
Publication(s):Kidd et al. 2010

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: 149 SVs from 43 studies. See in: genome view

Remapped(Score: Perfect):86,259,792-86,259,796

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv475165	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000012.12	Chr12	86,259,792	86,259,796
nsv475165	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000012.11	Chr12	86,653,570	86,653,574
nsv475165	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000012.10	Chr12	85,177,701	85,177,705

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv3019976	complex substitution	NA19240	Sequencing	Sequence alignment	627

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv3019976	Remapped	Perfect	GRCh38.p12	First Pass	NC_000012.12	Chr12	86,259,792	86,259,796
nssv3019976	Remapped	Perfect	GRCh37.p13	First Pass	NC_000012.11	Chr12	86,653,570	86,653,574
nssv3019976	Submitted genomic		NCBI36 (hg18)		NC_000012.10	Chr12	85,177,701	85,177,705

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

You are here: NCBI