A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596038



Internal ID16383447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:164482840..164542796hg38UCSC Ensembl
Innerchr4:165403992..165463948hg19UCSC Ensembl
Innerchr4:165623442..165683398hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3859957
hg1959957
hg1859957
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1010740
Samples
Known GenesMIR5684
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596038
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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