A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526901



Internal ID15107508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:35188374..35189113hg38UCSC Ensembl
Innerchr5:35188476..35189215hg19UCSC Ensembl
Innerchr5:35224233..35224972hg18UCSC Ensembl
Innerchr5:35224233..35224972hg17UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg38740
hg19740
hg18740
hg17740
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703261
Samples
Known GenesPRLR
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526901
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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