A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1002275



Internal ID15949545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:69745401..69810356hg38UCSC Ensembl
Innerchr4:70611119..70676074hg19UCSC Ensembl
Innerchr4:70645708..70710663hg18UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3864956
hg1964956
hg1864956
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv594641
Supporting Variants
Samples
Known GenesSULT1B1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1002275
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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