A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564127



Internal ID16351536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:27454979..27558719hg38UCSC Ensembl
Innerchr14:27924185..28027925hg19UCSC Ensembl
Innerchr14:26994025..27097765hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38103741
hg19103741
hg18103741
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv825069, nssv825068
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564127
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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