A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008191



Internal ID19097410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:112383718..112396146hg38UCSC Ensembl
Innerchr3:112102565..112114993hg19UCSC Ensembl
Innerchr3:113585255..113597683hg18UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg3812429
hg1912429
hg1812429
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4839n100
Supporting Variantsnssv3604436
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)nsv1008191
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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