A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3584780



Internal ID18883061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:40356606..40380041hg38UCSC Ensembl
Innerchr20:38985246..39008681hg19UCSC Ensembl
Innerchr20:38418660..38442095hg18UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3823436
hg1923436
hg1823436
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1066991
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)nssv3584780
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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