A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426055



Internal ID21083608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:98007623..98013565hg38UCSC Ensembl
chr8:99019851..99025793hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg385943
hg195943
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173580
Samples
Known GenesMATN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426055
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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