A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564912



Internal ID20937983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:60636930..60637546hg38UCSC Ensembl
chr8:61549489..61550105hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38617
hg19617
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278382
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564912
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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