A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056668



Internal ID19145887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:26239488..26297668hg38UCSC Ensembl
Innerchr20:26220124..26278304hg19UCSC Ensembl
Innerchr20:26168124..26226304hg18UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg3858181
hg1958181
hg1858181
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3584701
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)nsv1056668
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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