A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596297



Internal ID16383706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:180614655..180649944hg38UCSC Ensembl
Innerchr4:181535808..181571097hg19UCSC Ensembl
Innerchr4:181772802..181808091hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3835290
hg1935290
hg1835290
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1017059
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596297
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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