A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516917



Internal ID15444210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:3123124..3125271hg38UCSC Ensembl
Innerchr10:3165316..3167463hg19UCSC Ensembl
Innerchr10:3155316..3157463hg18UCSC Ensembl
Innerchr10:3155316..3157463hg17UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg382148
hg192148
hg182148
hg172148
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv683158, nssv690234, nssv654985, nssv691215, nssv676842
Samples
Known GenesPFKP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516917
Frequency
Sample Size2026
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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