A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv708536



Internal ID15655806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:1324404..1351367hg38UCSC Ensembl
Innerchr1:1259784..1286747hg19UCSC Ensembl
Innerchr1:1249647..1276610hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3826964
hg1926964
hg1826964
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv544975
Supporting Variants
Samples
Known GenesCPSF3L, DVL1, GLTPD1, MIR6808, TAS1R3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv708536
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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