A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573976



Internal ID20947047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89010792..89084402hg38UCSC Ensembl
chr6:89720511..89794121hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3873611
hg1973611
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274908
Samples
Known GenesPNRC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573976
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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