A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061301



Internal ID19150520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:16026844..16116425hg38UCSC Ensembl
Innerchr20:16007489..16097070hg19UCSC Ensembl
Innerchr20:15955489..16045070hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3889582
hg1989582
hg1889582
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3737168
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)nsv1061301
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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