A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv827846



Internal ID16121802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:48321920..48435852hg38UCSC Ensembl
Innerchr14:48791123..48905055hg19UCSC Ensembl
Innerchr14:47860873..47974805hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38113933
hg19113933
hg18113933
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564817
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)nssv827846
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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