A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061217



Internal ID19150436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:21895090..21925845hg38UCSC Ensembl
Innerchr20:21875728..21906483hg19UCSC Ensembl
Innerchr20:21823728..21854483hg18UCSC Ensembl
Cytoband20p11.22
Allele length
AssemblyAllele length
hg3830756
hg1930756
hg1830756
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3584652
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)nsv1061217
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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