A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568970



Internal ID20942041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:146014527..146095565hg38UCSC Ensembl
chr6:146335663..146416701hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg3881039
hg1981039
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273193
Samples
Known GenesGRM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568970
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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