A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170273



Internal ID21314334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:14684529..14685995hg38UCSC Ensembl
Outerchr21:14682621..14688400hg38UCSC Ensembl
Innerchr21:16056850..16058316hg19UCSC Ensembl
Outerchr21:16054942..16060721hg19UCSC Ensembl
Innerchr21:14978721..14980187hg18UCSC Ensembl
Outerchr21:14976813..14982592hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg385780
hg195780
hg185780
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14250212
SamplesPML_4
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170273
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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