A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565624



Internal ID16006347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:94494633..94512931hg38UCSC Ensembl
Innerchr14:94960970..94979268hg19UCSC Ensembl
Innerchr14:94030723..94049021hg18UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg3818299
hg1918299
hg1818299
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148962
SamplesHGDP00851
Known GenesSERPINA12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565624
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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