A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv708532



Internal ID15655802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:1294063..1351426hg38UCSC Ensembl
Innerchr1:1229443..1286806hg19UCSC Ensembl
Innerchr1:1219306..1276669hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3857364
hg1957364
hg1857364
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv544971
Supporting Variants
Samples
Known GenesACAP3, CPSF3L, DVL1, GLTPD1, MIR6726, MIR6727, MIR6808, PUSL1, TAS1R3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv708532
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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