A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv996877



Internal ID16290833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:44953947..45002970hg38UCSC Ensembl
Innerchr4:44955964..45004987hg19UCSC Ensembl
Innerchr4:44650721..44699744hg18UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3849024
hg1949024
hg1849024
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv594099
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv996877
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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