A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055699



Internal ID18798230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:49529680..49618211hg38UCSC Ensembl
Innerchr20:48146217..48234748hg19UCSC Ensembl
Innerchr20:47579624..47668155hg18UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3888532
hg1988532
hg1888532
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4323n100
Supporting Variantsnssv3584957
Samples
Known GenesPTGIS
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055699
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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