A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703751



Internal ID15440403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:10342038..10462509hg38UCSC Ensembl
Innerchr8:10199548..10320019hg19UCSC Ensembl
Innerchr8:10236958..10357429hg18UCSC Ensembl
Innerchr8:10236958..10357429hg17UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38120472
hg19120472
hg18120472
hg17120472
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527326
Supporting Variants
Samples
Known GenesMSRA
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703751
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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