A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057674



Internal ID19146893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:16583997..16612564hg38UCSC Ensembl
Innerchr20:16564642..16593209hg19UCSC Ensembl
Innerchr20:16512642..16541209hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3828568
hg1928568
hg1828568
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4280n100
Supporting Variantsnssv3599642
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)nsv1057674
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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