A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067296



Internal ID19156515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:26229804..26324931hg38UCSC Ensembl
Innerchr20:26210440..26305567hg19UCSC Ensembl
Innerchr20:26158440..26253567hg18UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg3895128
hg1995128
hg1895128
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4293n100
Supporting Variantsnssv3584700, nssv3584699, nssv3584695, nssv3584698, nssv3584697, nssv3584696, nssv3584694
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)nsv1067296
Frequency
Sample Size11257
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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