A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517630



Internal ID15098237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:2632486..3097509hg38UCSC Ensembl
Innerchr10:2674678..3139701hg19UCSC Ensembl
Innerchr10:2664678..3129701hg18UCSC Ensembl
Innerchr10:2664678..3129701hg17UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg38465024
hg19465024
hg18465024
hg17465024
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv667044, nssv685475, nssv679577, nssv661593, nssv670928, nssv687391, nssv656112, nssv697914, nssv702153, nssv667337, nssv705918, nssv681418, nssv652592, nssv671462, nssv662458, nssv682637, nssv687253
Samples
Known GenesPFKP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517630
Frequency
Sample Size2026
Observed Gain11
Observed Loss6
Observed Complex0
Frequencyn/a


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