A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595925



Internal ID16383334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:161024150..161082472hg38UCSC Ensembl
Innerchr4:161945302..162003624hg19UCSC Ensembl
Innerchr4:162164752..162223074hg18UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg3858323
hg1958323
hg1858323
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9351n54
Supporting Variantsnssv1010249, nssv1010250, nssv1010248, nssv1152957, nssv1152956
SamplesNINDS_155, HGDP00527
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595925
Frequency
Sample Size17421
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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