A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006537



Internal ID19095754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:112380800..112395969hg38UCSC Ensembl
Innerchr3:112099647..112114816hg19UCSC Ensembl
Innerchr3:113582337..113597506hg18UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg3815170
hg1915170
hg1815170
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4838n100
Supporting Variantsnssv3604423
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)nsv1006537
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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