A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1001897



Internal ID15949167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68528033..68585366hg38UCSC Ensembl
Innerchr4:69393751..69451084hg19UCSC Ensembl
Innerchr4:69076346..69133679hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3857334
hg1957334
hg1857334
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv594528
Supporting Variants
Samples
Known GenesUGT2B17
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1001897
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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