A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064902



Internal ID18807433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:24767657..24797575hg38UCSC Ensembl
Innerchr22:25163624..25193542hg19UCSC Ensembl
Innerchr22:23493624..23523542hg18UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3829919
hg1929919
hg1829919
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3588055
Samples
Known GenesPIWIL3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064902
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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