A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575191



Internal ID20948262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:97718745..97719435hg38UCSC Ensembl
chr8:98730973..98731663hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38691
hg19691
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7430n223
Supporting Variantsnssv18279201
Samples
Known GenesMTDH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575191
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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