A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062766



Internal ID19151985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:30185664..30400778hg38UCSC Ensembl
Innerchr20:29420340..29635454hg19UCSC Ensembl
Innerchr20:28034001..28249115hg18UCSC Ensembl
Cytoband20q11.1
Allele length
AssemblyAllele length
hg38215115
hg19215115
hg18215115
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4296n100
Supporting Variantsnssv3584724
Samples
Known GenesFRG1B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062766
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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