A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066625



Internal ID19155844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:20920683..20948518hg38UCSC Ensembl
Innerchr22:21274971..21302806hg19UCSC Ensembl
Innerchr22:19604971..19632806hg18UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3827836
hg1927836
hg1827836
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3587384
Samples
Known GenesCRKL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066625
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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