A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998316



Internal ID19157852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:112383718..112397796hg38UCSC Ensembl
Innerchr3:112102565..112116643hg19UCSC Ensembl
Innerchr3:113585255..113599333hg18UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg3814079
hg1914079
hg1814079
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4839n100
Supporting Variantsnssv3604437
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998316
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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