A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv832173



Internal ID15779443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:89416879..89416981hg38UCSC Ensembl
Innerchr14:89883223..89883325hg19UCSC Ensembl
Innerchr14:88952976..88953078hg18UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38103
hg19103
hg18103
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565514
Supporting Variants
Samples
Known GenesFOXN3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv832173
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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