A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148950



Internal ID15873174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:38222364..38283547hg38UCSC Ensembl
Innerchr14:38691569..38752752hg19UCSC Ensembl
Innerchr14:37761320..37822503hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3861184
hg1961184
hg1861184
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564399
Supporting Variants
SamplesHGDP00137
Known GenesCLEC14A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148950
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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