A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018955



Internal ID18761488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:120344223..120466319hg38UCSC Ensembl
Innerchr5:119679918..119802014hg19UCSC Ensembl
Innerchr5:119707817..119829913hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38122097
hg19122097
hg18122097
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3647983, nssv3647982
Samples
Known GenesPRR16
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018955
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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