A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575183



Internal ID20948254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:23965527..24582482hg38UCSC Ensembl
chr8:23823040..24439995hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38616956
hg19616956
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18277522
Samples
Known GenesADAM28, ADAM7, ADAMDEC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575183
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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