A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150725



Internal ID15854585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:53495457..53607946hg38UCSC Ensembl
Innerchr2:53722595..53835083hg19UCSC Ensembl
Innerchr2:53576099..53688587hg18UCSC Ensembl
Cytoband2p16.2
Allele length
AssemblyAllele length
hg38112490
hg19112489
hg18112489
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv582010
Supporting Variants
Samples1780862212_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150725
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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