A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064120



Internal ID19153339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:19089508..19117867hg38UCSC Ensembl
Innerchr20:19070152..19098511hg19UCSC Ensembl
Innerchr20:19018152..19046511hg18UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg3828360
hg1928360
hg1828360
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4284n100
Supporting Variantsnssv3584647, nssv3584646
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)nsv1064120
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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