A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570779



Internal ID20943850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:132991570..132992199hg38UCSC Ensembl
chr8:134003815..134004444hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38630
hg19630
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7499n223
Supporting Variantsnssv18277152
Samples
Known GenesTG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570779
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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