A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019099



Internal ID19108317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:181249107..181292789hg38UCSC Ensembl
Innerchr5:180676107..180719790hg19UCSC Ensembl
Innerchr5:180608713..180652396hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3843683
hg1943684
hg1843684
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3650354
Samples
Known GenesTRIM52, TRIM52-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019099
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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