A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3599615



Internal ID18551210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14952238..15141996hg38UCSC Ensembl
Innerchr20:14932884..15122642hg19UCSC Ensembl
Innerchr20:14880884..15070642hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38189759
hg19189759
hg18189759
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056236
Supporting Variants
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)nssv3599615
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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