A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596307



Internal ID16037030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:181379580..181556233hg38UCSC Ensembl
Innerchr4:182300733..182477386hg19UCSC Ensembl
Innerchr4:182537727..182714380hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38176654
hg19176654
hg18176654
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1017750
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596307
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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