A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv938049



Internal ID15885319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14568030..14629643hg38UCSC Ensembl
Innerchr20:14548676..14610289hg19UCSC Ensembl
Innerchr20:14496676..14558289hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3861614
hg1961614
hg1861614
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585450
Supporting Variants
Samples
Known GenesMACROD2, MACROD2-IT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv938049
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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