A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564695



Internal ID16352104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:44585574..44660661hg38UCSC Ensembl
Innerchr14:45054777..45129864hg19UCSC Ensembl
Innerchr14:44124527..44199614hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg3875088
hg1975088
hg1875088
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv827610
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564695
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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