A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569302



Internal ID16356711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:44782321..44806944hg38UCSC Ensembl
Innerchr15:45074519..45099142hg19UCSC Ensembl
Innerchr15:42861811..42886434hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3824624
hg1924624
hg1824624
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149590
Samples1780854205_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569302
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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