A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516811



Internal ID15097418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:3108122..3113598hg38UCSC Ensembl
Innerchr10:3150314..3155790hg19UCSC Ensembl
Innerchr10:3140314..3145790hg18UCSC Ensembl
Innerchr10:3140314..3145790hg17UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg385477
hg195477
hg185477
hg175477
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv691864, nssv695303, nssv671083, nssv663438
Samples
Known GenesPFKP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516811
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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