A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv588077



Internal ID16028800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:16674094..16972076hg38UCSC Ensembl
Innerchr22:17154984..17452966hg19UCSC Ensembl
Innerchr22:15534984..15832966hg18UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg38297983
hg19297983
hg18297983
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv949517
Samples
Known GenesANKRD62P1-PARP4P3, GAB4, HSFY1P1, XKR3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv588077
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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