A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150238



Internal ID15874473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:77750136..77812540hg38UCSC Ensembl
Innerchr2:77977262..78039666hg19UCSC Ensembl
Innerchr2:77830770..77893174hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3862405
hg1962405
hg1862405
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv582263
Supporting Variants
SamplesHGDP00544
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150238
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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