A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525336



Internal ID15452629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:34625243..34669501hg38UCSC Ensembl
Innerchr10:34914171..34958429hg19UCSC Ensembl
Innerchr10:34954177..34998435hg18UCSC Ensembl
Innerchr10:34954177..34998435hg17UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3844259
hg1944259
hg1844259
hg1744259
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701454
Samples
Known GenesPARD3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525336
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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