A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560745



Internal ID20933816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:96831898..96832570hg38UCSC Ensembl
chr6:97279774..97280446hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38673
hg19673
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272778
Samples
Known GenesGPR63
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560745
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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