A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066628



Internal ID19155847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:52268432..52303502hg38UCSC Ensembl
Innerchr20:50884971..50920041hg19UCSC Ensembl
Innerchr20:50318378..50353448hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3835071
hg1935071
hg1835071
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3731364
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)nsv1066628
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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