A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515521



Internal ID15443132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:16463718..16476408hg38UCSC Ensembl
Innerchr10:16505717..16518407hg19UCSC Ensembl
Innerchr10:16545723..16558413hg18UCSC Ensembl
Innerchr10:16545723..16558413hg17UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3812691
hg1912691
hg1812691
hg1712691
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697041, nssv653446, nssv658424
Samples
Known GenesPTER
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515521
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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