A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060929



Internal ID18803460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:31706715..31780874hg38UCSC Ensembl
Innerchr22:32102701..32176860hg19UCSC Ensembl
Innerchr22:30432701..30506860hg18UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg3874160
hg1974160
hg1874160
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3734198
Samples
Known GenesDEPDC5, PRR14L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060929
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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