A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565896



Internal ID16353305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101707701..101720203hg38UCSC Ensembl
Innerchr14:102174038..102186540hg19UCSC Ensembl
Innerchr14:101243791..101256293hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3812503
hg1912503
hg1812503
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3921n54
Supporting Variantsnssv833755
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565896
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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