A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567851



Internal ID20940922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:74996738..74998537hg38UCSC Ensembl
chr8:75908973..75910772hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278715
Samples
Known GenesCRISPLD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567851
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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