A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv599404



Internal ID16386813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:113629448..113645831hg38UCSC Ensembl
Innerchr5:112965145..112981528hg19UCSC Ensembl
Innerchr5:112993044..113009427hg18UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg3816384
hg1916384
hg1816384
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10011n54
Supporting Variantsnssv1040402, nssv1040401
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv599404
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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