A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424187



Internal ID21081740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:97695965..97696353hg38UCSC Ensembl
chr8:98708193..98708581hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38389
hg19389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173553
Samples
Known GenesMTDH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424187
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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