A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564199



Internal ID16351608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:34665980..34698156hg38UCSC Ensembl
Innerchr14:35135186..35167362hg19UCSC Ensembl
Innerchr14:34204937..34237113hg18UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3832177
hg1932177
hg1832177
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv825162
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564199
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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