A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv827621



Internal ID16121577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:44702142..44755372hg38UCSC Ensembl
Innerchr14:45171345..45224575hg19UCSC Ensembl
Innerchr14:44241095..44294325hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg3853231
hg1953231
hg1853231
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564706
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)nssv827621
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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