A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3599377



Internal ID18897658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:11398836..11424654hg38UCSC Ensembl
Innerchr20:11379484..11405302hg19UCSC Ensembl
Innerchr20:11327484..11353302hg18UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg3825819
hg1925819
hg1825819
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1061567
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)nssv3599377
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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