A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594009



Internal ID16034732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:38678565..38701308hg38UCSC Ensembl
Innerchr4:38680186..38702929hg19UCSC Ensembl
Innerchr4:38356581..38379324hg18UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3822744
hg1922744
hg1822744
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153458
Samples1780862573_A
Known GenesKLF3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594009
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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