A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015063



Internal ID18757598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:161200519..161306282hg38UCSC Ensembl
Innerchr3:160918307..161024070hg19UCSC Ensembl
Innerchr3:162401001..162506764hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38105764
hg19105764
hg18105764
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3606407
Samples
Known GenesNMD3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015063
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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