A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064726



Internal ID19153945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:20936642..20948157hg38UCSC Ensembl
Innerchr22:21290930..21302445hg19UCSC Ensembl
Innerchr22:19620930..19632445hg18UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3811516
hg1911516
hg1811516
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4485n100
Supporting Variantsnssv3587388
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)nsv1064726
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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