A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009145



Internal ID19098363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:117369686..117390341hg38UCSC Ensembl
Innerchr3:117088533..117109188hg19UCSC Ensembl
Innerchr3:118571223..118591878hg18UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3820656
hg1920656
hg1820656
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4843n100
Supporting Variantsnssv3604486
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)nsv1009145
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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