A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3593111



Internal ID18891392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21199919..21302104hg38UCSC Ensembl
Innerchr3:21241411..21343596hg19UCSC Ensembl
Innerchr3:21216415..21318600hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38102186
hg19102186
hg18102186
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1013139
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)nssv3593111
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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