A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011615



Internal ID19100832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:163407108..163592404hg38UCSC Ensembl
Innerchr3:163124896..163310192hg19UCSC Ensembl
Innerchr3:164607590..164792886hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38185297
hg19185297
hg18185297
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3614526
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)nsv1011615
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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