A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148701



Internal ID15873115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:40935888..41070570hg38UCSC Ensembl
Innerchr14:41405093..41539775hg19UCSC Ensembl
Innerchr14:40474843..40609525hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38134683
hg19134683
hg18134683
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564470
Supporting Variants
SamplesHGDP00127
Known GenesLOC644919
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148701
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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