A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575400



Internal ID20948471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:97892161..97893718hg38UCSC Ensembl
chr8:98904389..98905946hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg381558
hg191558
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279214
Samples
Known GenesMATN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575400
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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