A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518657



Internal ID15445950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:103717405..103724026hg38UCSC Ensembl
Innerchr10:105477163..105483784hg19UCSC Ensembl
Innerchr10:105467153..105473774hg18UCSC Ensembl
Innerchr10:105467153..105473774hg17UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg386622
hg196622
hg186622
hg176622
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696107
Samples
Known GenesSH3PXD2A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518657
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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