A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169853



Internal ID21313664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:168119873..168122176hg38UCSC Ensembl
Outerchr1:168113769..168125471hg38UCSC Ensembl
Innerchr1:168089111..168091414hg19UCSC Ensembl
Outerchr1:168083007..168094709hg19UCSC Ensembl
Innerchr1:166355735..166358038hg18UCSC Ensembl
Outerchr1:166349631..166361333hg18UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3811703
hg1911703
hg1811703
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14241437
SamplesMLY_4
Known GenesGPR161
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169853
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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