A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061705



Internal ID19150924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14349383..14449958hg38UCSC Ensembl
Innerchr20:14330029..14430604hg19UCSC Ensembl
Innerchr20:14278029..14378604hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38100576
hg19100576
hg18100576
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4249n100
Supporting Variantsnssv3734879
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)nsv1061705
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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