A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169778



Internal ID21313589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:45831529..45834375hg38UCSC Ensembl
Outerchr21:45830325..45842899hg38UCSC Ensembl
Innerchr21:47251443..47254289hg19UCSC Ensembl
Outerchr21:47250239..47262813hg19UCSC Ensembl
Innerchr21:46075871..46078717hg18UCSC Ensembl
Outerchr21:46074667..46087241hg18UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3812575
hg1912575
hg1812575
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14248172
SamplesNGO_6
Known GenesLOC100129027
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169778
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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