A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6571834



Internal ID20944905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:146282641..146288910hg38UCSC Ensembl
chr6:146603777..146610046hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg386270
hg196270
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18273196
Samples
Known GenesGRM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6571834
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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