A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565625



Internal ID16006348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:94567019..94603850hg38UCSC Ensembl
Innerchr14:95033356..95070187hg19UCSC Ensembl
Innerchr14:94103109..94139940hg18UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg3836832
hg1936832
hg1836832
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv832702
Samples
Known GenesSERPINA4, SERPINA5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565625
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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