A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057619



Internal ID19146838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:15321244..15337332hg38UCSC Ensembl
Innerchr20:15301890..15317978hg19UCSC Ensembl
Innerchr20:15249890..15265978hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3816089
hg1916089
hg1816089
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4278n100
Supporting Variantsnssv3599626, nssv3599627
Samples
Known GenesMACROD2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057619
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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