A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv832703



Internal ID15779973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:94583971..94592873hg38UCSC Ensembl
Innerchr14:95050308..95059210hg19UCSC Ensembl
Innerchr14:94120061..94128963hg18UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg388903
hg198903
hg188903
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565626
Supporting Variants
Samples
Known GenesSERPINA5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv832703
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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