A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056353



Internal ID19145572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:26242063..26324931hg38UCSC Ensembl
Innerchr20:26222699..26305567hg19UCSC Ensembl
Innerchr20:26170699..26253567hg18UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg3882869
hg1982869
hg1882869
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4293n100
Supporting Variantsnssv3584709, nssv3584708, nssv3584707, nssv3584703, nssv3584706, nssv3584705, nssv3584710, nssv3584704
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)nsv1056353
Frequency
Sample Size11257
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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