A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3522612



Internal ID18474207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:60211987..60293736hg38UCSC Ensembl
Innerchr11:59979460..60061209hg19UCSC Ensembl
Innerchr11:59736036..59817785hg18UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3881750
hg1981750
hg1881750
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053558
Supporting Variants
Samples
Known GenesMS4A4A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3522612
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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