A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148964



Internal ID15875166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:94975944..95029254hg38UCSC Ensembl
Innerchr14:95442281..95495591hg19UCSC Ensembl
Innerchr14:94512034..94565344hg18UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg3853311
hg1953311
hg1853311
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565629
Supporting Variants
SamplesHGDP00645
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148964
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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