A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056672



Internal ID19145891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:20928403..20948062hg38UCSC Ensembl
Innerchr22:21282691..21302350hg19UCSC Ensembl
Innerchr22:19612691..19632350hg18UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3819660
hg1919660
hg1819660
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4484n100
Supporting Variantsnssv3587386
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)nsv1056672
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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