A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169801



Internal ID21313612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:127581966..127681663hg38UCSC Ensembl
Outerchr3:127577947..127684175hg38UCSC Ensembl
Innerchr3:127300809..127400506hg19UCSC Ensembl
Outerchr3:127296790..127403018hg19UCSC Ensembl
Innerchr3:128783499..128883196hg18UCSC Ensembl
Outerchr3:128779480..128885708hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38106229
hg19106229
hg18106229
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14240888
SamplesNGO_23
Known GenesABTB1, MCM2, PODXL2, TPRA1
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169801
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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