A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv982549



Internal ID16276505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:183396220..183424756hg38UCSC Ensembl
Innerchr3:183114008..183142544hg19UCSC Ensembl
Innerchr3:184596702..184625238hg18UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg3828537
hg1928537
hg1828537
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592655
Supporting Variants
Samples
Known GenesMCF2L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv982549
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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