A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564775



Internal ID20937846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:139038075..139038944hg38UCSC Ensembl
chr6:139359212..139360081hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38870
hg19870
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272486
Samples
Known GenesABRACL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564775
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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