A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038982



Internal ID19128201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:89547309..89692837hg38UCSC Ensembl
Innerchr13:90199563..90345091hg19UCSC Ensembl
Innerchr13:88997564..89143092hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38145529
hg19145529
hg18145529
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525469
Samples
Known GenesLINC00353
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038982
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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