A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv832176



Internal ID16126132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:92384977..92410493hg38UCSC Ensembl
Innerchr14:92851321..92876837hg19UCSC Ensembl
Innerchr14:91921074..91946590hg18UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3825517
hg1925517
hg1825517
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565521
Supporting Variants
Samples
Known GenesSLC24A4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv832176
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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