A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055943



Internal ID19145162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:15324612..15337332hg38UCSC Ensembl
Innerchr20:15305258..15317978hg19UCSC Ensembl
Innerchr20:15253258..15265978hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3812721
hg1912721
hg1812721
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4278n100
Supporting Variantsnssv3599630, nssv3599628, nssv3599629
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)nsv1055943
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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