A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148594



Internal ID15856080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:44615589..44732341hg38UCSC Ensembl
Innerchr14:45084792..45201544hg19UCSC Ensembl
Innerchr14:44154542..44271294hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38116753
hg19116753
hg18116753
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564699
Supporting Variants
Samples1798860587_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148594
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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