A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv832167



Internal ID15779437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:87928587..87953938hg38UCSC Ensembl
Innerchr14:88394931..88420282hg19UCSC Ensembl
Innerchr14:87464684..87490035hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3825352
hg1925352
hg1825352
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565508
Supporting Variants
Samples
Known GenesGALC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv832167
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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