A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569970



Internal ID20943041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:95760239..95762230hg38UCSC Ensembl
chr8:96772467..96774458hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg381992
hg191992
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279167
Samples
Known GenesLOC100616530
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569970
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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