A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432855



Internal ID21090408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:77229701..77230300hg38UCSC Ensembl
chr8:78141937..78142536hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18171436
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432855
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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