A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060202



Internal ID18802733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:54035511..54046023hg38UCSC Ensembl
Innerchr20:52652050..52662562hg19UCSC Ensembl
Innerchr20:52085457..52095969hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3810513
hg1910513
hg1810513
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4330n100
Supporting Variantsnssv3587560, nssv3587561
Samples
Known GenesBCAS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060202
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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