A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420622



Internal ID21078175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:97666966..97678952hg38UCSC Ensembl
chr8:98679194..98691180hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3811987
hg1911987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173547
Samples
Known GenesMTDH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420622
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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