A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524046



Internal ID15451339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:34170422..34652206hg38UCSC Ensembl
Innerchr10:34459350..34941134hg19UCSC Ensembl
Innerchr10:34499356..34981140hg18UCSC Ensembl
Innerchr10:34499356..34981140hg17UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38481785
hg19481785
hg18481785
hg17481785
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699910
Samples
Known GenesPARD3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524046
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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