A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596361



Internal ID16383770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:184825633..184826384hg38UCSC Ensembl
Innerchr4:185746787..185747538hg19UCSC Ensembl
Innerchr4:185983781..185984532hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38752
hg19752
hg18752
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1017969
Samples
Known GenesACSL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596361
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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