A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572542



Internal ID20945613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:48622203..48622785hg38UCSC Ensembl
chr8:49534763..49535345hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg38583
hg19583
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278137
Samples
Known GenesLOC101929217, LOC101929268
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572542
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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