A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032559



Internal ID19121781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:167643883..167783679hg38UCSC Ensembl
Innerchr5:167070888..167210684hg19UCSC Ensembl
Innerchr5:167003466..167143262hg18UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38139797
hg19139797
hg18139797
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3649117
Samples
Known GenesTENM2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032559
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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