A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169935



Internal ID21313996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:120155471..120176874hg38UCSC Ensembl
Outerchr3:120150751..120182927hg38UCSC Ensembl
Innerchr3:119874318..119895721hg19UCSC Ensembl
Outerchr3:119869598..119901774hg19UCSC Ensembl
Innerchr3:121357008..121378411hg18UCSC Ensembl
Outerchr3:121352288..121384464hg18UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg3832177
hg1932177
hg1832177
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14248173
SamplesNGO_25
Known GenesGPR156
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169935
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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