A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705056



Internal ID15095022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133452885..133464689hg38UCSC Ensembl
Innerchr10:135266389..135278193hg19UCSC Ensembl
Innerchr10:135116379..135128183hg18UCSC Ensembl
Innerchr10:135155270..135167074hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3811805
hg1911805
hg1811805
hg1711805
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517180
Supporting Variants
Samples
Known GenesSCART1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705056
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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