A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3733105



Internal ID19031386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:22398333..22879666hg38UCSC Ensembl
Innerchr22:22752668..23221846hg19UCSC Ensembl
Innerchr22:21082668..21551846hg18UCSC Ensembl
Cytoband22q11.22
Allele length
AssemblyAllele length
hg38481334
hg19469179
hg18469179
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058320
Supporting Variants
Samples
Known GenesGGTLC2, LOC648691, MIR650, POM121L1P, PRAME, ZNF280A, ZNF280B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3733105
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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