A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560526



Internal ID20933597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99419566..99420185hg38UCSC Ensembl
chr6:99867442..99868061hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg38620
hg19620
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6335n223
Supporting Variantsnssv18272829
Samples
Known GenesPNISR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560526
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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