A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056639



Internal ID19145858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:30185664..30258050hg38UCSC Ensembl
Innerchr20:29420340..29492726hg19UCSC Ensembl
Innerchr20:28034001..28106387hg18UCSC Ensembl
Cytoband20q11.1
Allele length
AssemblyAllele length
hg3872387
hg1972387
hg1872387
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4294n100
Supporting Variantsnssv3584718
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)nsv1056639
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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