A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1003196



Internal ID15950466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:92269047..92470100hg38UCSC Ensembl
Innerchr4:93190198..93391251hg19UCSC Ensembl
Innerchr4:93409221..93610274hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38201054
hg19201054
hg18201054
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv594868
Supporting Variants
Samples
Known GenesGRID2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1003196
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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