A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv829047



Internal ID16123003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:70221635..70224160hg38UCSC Ensembl
Innerchr14:70688352..70690877hg19UCSC Ensembl
Innerchr14:69758105..69760630hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg382526
hg192526
hg182526
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565030
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv829047
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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