A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3599660



Internal ID18897941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:16587417..16605899hg38UCSC Ensembl
Innerchr20:16568062..16586544hg19UCSC Ensembl
Innerchr20:16516062..16534544hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3818483
hg1918483
hg1818483
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059010
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)nssv3599660
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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