A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv832708



Internal ID16126664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:95613538..95616356hg38UCSC Ensembl
Innerchr14:96079875..96082693hg19UCSC Ensembl
Innerchr14:95149628..95152446hg18UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg382819
hg192819
hg182819
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565633
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)nssv832708
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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