A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv826657



Internal ID16120613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:40248639..40319935hg38UCSC Ensembl
Innerchr14:40717843..40789139hg19UCSC Ensembl
Innerchr14:39787593..39858889hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3871297
hg1971297
hg1871297
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564455
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)nssv826657
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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