A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565891



Internal ID16353300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101707701..101712964hg38UCSC Ensembl
Innerchr14:102174038..102179301hg19UCSC Ensembl
Innerchr14:101243791..101249054hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg385264
hg195264
hg185264
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3923n54
Supporting Variantsnssv833741
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565891
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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