A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416020



Internal ID21073573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:21948576..21949198hg38UCSC Ensembl
chr8:21806087..21806709hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38623
hg19623
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167065
Samples
Known GenesXPO7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416020
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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