A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148939



Internal ID15878666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:29149561..29196263hg38UCSC Ensembl
Innerchr14:29618767..29665469hg19UCSC Ensembl
Innerchr14:28688518..28735220hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3846703
hg1946703
hg1846703
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564161
Supporting Variants
SamplesHGDP01238
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148939
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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