A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3588052



Internal ID18886333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:24668997..24685359hg38UCSC Ensembl
Innerchr22:25064964..25081326hg19UCSC Ensembl
Innerchr22:23394964..23411326hg18UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3816363
hg1916363
hg1816363
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059697
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3588052
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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