A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv832732



Internal ID16126688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:96707232..96709345hg38UCSC Ensembl
Innerchr14:97173569..97175682hg19UCSC Ensembl
Innerchr14:96243322..96245435hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg382114
hg192114
hg182114
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565652
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)nssv832732
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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