A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526559



Internal ID15107166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:168748286..168753076hg38UCSC Ensembl
Innerchr5:168175291..168180081hg19UCSC Ensembl
Innerchr5:168107869..168112659hg18UCSC Ensembl
Innerchr5:168107869..168112659hg17UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg384791
hg194791
hg184791
hg174791
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv360n21
Supporting Variantsnssv702874
Samples
Known GenesSLIT3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526559
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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