A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662309



Internal ID15398961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:4395562..4395627hg38UCSC Ensembl
Innerchr10:4437754..4437819hg19UCSC Ensembl
Innerchr10:4427754..4427819hg18UCSC Ensembl
Innerchr10:4427754..4427819hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3866
hg1966
hg1866
hg1766
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516066
Supporting Variants
Samples
Known GenesLINC00703
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv662309
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer