A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001259



Internal ID19090476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:145508846..145537008hg38UCSC Ensembl
Innerchr3:145226633..145254795hg19UCSC Ensembl
Innerchr3:146709323..146737485hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3828163
hg1928163
hg1828163
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4916n100
Supporting Variantsnssv3741488
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)nsv1001259
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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