A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv994301



Internal ID16288257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:20405968..20416685hg38UCSC Ensembl
Innerchr4:20407591..20418308hg19UCSC Ensembl
Innerchr4:20016689..20027406hg18UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg3810718
hg1910718
hg1810718
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593795
Supporting Variants
Samples
Known GenesSLIT2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv994301
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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