A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066991



Internal ID19156210
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 StatusM
Merged Variants
Supporting Variantsnssv3584780
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)nsv1066991
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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