A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419794



Internal ID21077347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:80148597..80191807hg38UCSC Ensembl
chr8:81060832..81104042hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3843211
hg1943211
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229759
Samples
Known GenesTPD52
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419794
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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