A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565865



Internal ID16353274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101457469..101458626hg38UCSC Ensembl
Innerchr14:101923806..101924963hg19UCSC Ensembl
Innerchr14:100993559..100994716hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg381158
hg191158
hg181158
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3916n54
Supporting Variantsnssv833683, nssv833684
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565865
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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