A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151618



Internal ID15527522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:36462343..36500149hg38UCSC Ensembl
Innerchr21:37834641..37872447hg19UCSC Ensembl
Innerchr21:36756511..36794317hg18UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg3837807
hg1937807
hg1837807
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv587470
Supporting Variants
SamplesHGDP00490
Known GenesCLDN14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151618
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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