A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005261



Internal ID19094478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:6082608..6573922hg38UCSC Ensembl
Innerchr3:6124295..6615609hg19UCSC Ensembl
Innerchr3:6099295..6590609hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38491315
hg19491315
hg18491315
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3591696
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)nsv1005261
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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