A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060934



Internal ID19150153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:16593105..16865315hg38UCSC Ensembl
Innerchr22:17073995..17346205hg19UCSC Ensembl
Innerchr22:15453995..15726205hg18UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg38272211
hg19272211
hg18272211
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4461n100
Supporting Variantsnssv3589319
Samples
Known GenesANKRD62P1-PARP4P3, HSFY1P1, TPTEP1, XKR3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060934
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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