A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565628



Internal ID16353037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:94935089..94962817hg38UCSC Ensembl
Innerchr14:95401426..95429154hg19UCSC Ensembl
Innerchr14:94471179..94498907hg18UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg3827729
hg1927729
hg1827729
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148963
SamplesHGDP01004
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565628
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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