A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv680332



Internal ID15070298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:1070426..1275912hg38UCSC Ensembl
Innerchr1:1005806..1211292hg19UCSC Ensembl
Innerchr1:995669..1201155hg18UCSC Ensembl
Innerchr1:1045729..1251215hg17UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38205487
hg19205487
hg18205487
hg17205487
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517709
Supporting Variants
Samples
Known GenesB3GALT6, C1orf159, FAM132A, LOC254099, MIR200A, MIR200B, MIR429, RNF223, SDF4, TNFRSF18, TNFRSF4, TTLL10, UBE2J2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv680332
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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