A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061714



Internal ID19150933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:30185664..30325927hg38UCSC Ensembl
Innerchr20:29420340..29560603hg19UCSC Ensembl
Innerchr20:28034001..28174264hg18UCSC Ensembl
Cytoband20q11.1
Allele length
AssemblyAllele length
hg38140264
hg19140264
hg18140264
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4295n100
Supporting Variantsnssv3584722
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061714
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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