A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv681592



Internal ID15071558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:89171845..89208346hg38UCSC Ensembl
Innerchr10:90931602..90968103hg19UCSC Ensembl
Innerchr10:90921582..90958083hg18UCSC Ensembl
Innerchr10:90921582..90958083hg17UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3836502
hg1936502
hg1836502
hg1736502
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517170
Supporting Variants
Samples
Known GenesCH25H
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv681592
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