A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151045



Internal ID15878639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:40578287..40621410hg38UCSC Ensembl
Innerchr2:40805427..40848550hg19UCSC Ensembl
Innerchr2:40658931..40702054hg18UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3843124
hg1943124
hg1843124
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581505
Supporting Variants
SamplesHGDP01237
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151045
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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