A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3731945



Internal ID18683540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:21960705..22219039hg38UCSC Ensembl
Innerchr22:22315077..22573431hg19UCSC Ensembl
Innerchr22:20645077..20903431hg18UCSC Ensembl
Cytoband22q11.22
Allele length
AssemblyAllele length
hg38258335
hg19258355
hg18258355
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056045
Supporting Variants
Samples
Known GenesTOP3B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3731945
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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