A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1003192



Internal ID16297148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:91471001..92301364hg38UCSC Ensembl
Innerchr4:92392152..93222515hg19UCSC Ensembl
Innerchr4:92611175..93441538hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38830364
hg19830364
hg18830364
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv594862
Supporting Variants
Samples
Known GenesCCSER1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1003192
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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