A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149484



Internal ID15877843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:27885392..27972675hg38UCSC Ensembl
Innerchr14:28354598..28441881hg19UCSC Ensembl
Innerchr14:27424438..27511721hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3887284
hg1987284
hg1887284
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564138
Supporting Variants
SamplesHGDP01053
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149484
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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