A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656901



Internal ID15393553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:6834935..6859324hg38UCSC Ensembl
Innerchr4:6836662..6861051hg19UCSC Ensembl
Innerchr4:6887563..6911952hg18UCSC Ensembl
Innerchr4:6954734..6979123hg17UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3824390
hg1924390
hg1824390
hg1724390
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519565
Supporting Variants
Samples
Known GenesKIAA0232
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv656901
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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