A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429631



Internal ID21087184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:97723244..97723592hg38UCSC Ensembl
chr8:98735472..98735820hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38349
hg19349
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173555
Samples
Known GenesMTDH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429631
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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