A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150407



Internal ID15872659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:18004324..18070689hg38UCSC Ensembl
Innerchr2:18185590..18251955hg19UCSC Ensembl
Innerchr2:18049071..18115436hg18UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg3866366
hg1966366
hg1866366
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581109
Supporting Variants
SamplesHGDP00007
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150407
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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