A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660951



Internal ID15397603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:9039746..9068825hg38UCSC Ensembl
Innerchr10:9081709..9110788hg19UCSC Ensembl
Innerchr10:9121715..9150794hg18UCSC Ensembl
Innerchr10:9121715..9150794hg17UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3829080
hg1929080
hg1829080
hg1729080
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520120
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660951
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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