A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5911301



Internal ID22686515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:97697098..97697166hg38UCSC Ensembl
chr8:98709326..98709394hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17430223
Samples
Known GenesMTDH
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5911301
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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