A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565049



Internal ID16352458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:72603947..72656563hg38UCSC Ensembl
Innerchr14:73070655..73123271hg19UCSC Ensembl
Innerchr14:72140408..72193024hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3852617
hg1952617
hg1852617
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148955
SamplesNINDS_198
Known GenesDPF3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565049
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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