A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169701



Internal ID21313512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:14787280..14797225hg38UCSC Ensembl
Outerchr21:14780425..14800414hg38UCSC Ensembl
Innerchr21:16159601..16169546hg19UCSC Ensembl
Outerchr21:16152746..16172735hg19UCSC Ensembl
Innerchr21:15081472..15091417hg18UCSC Ensembl
Outerchr21:15074617..15094606hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg3819990
hg1919990
hg1819990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14249561
SamplesMLY_12
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169701
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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