A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596371



Internal ID16383780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:185247233..185306378hg38UCSC Ensembl
Innerchr4:186168387..186227532hg19UCSC Ensembl
Innerchr4:186405381..186464526hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3859146
hg1959146
hg1859146
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1017980
Samples
Known GenesSNX25
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596371
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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