A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542187



Internal ID20915451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:50012496..50013555hg38UCSC Ensembl
chr3:50049929..50050988hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg381060
hg191060
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262847
Samples
Known GenesRBM6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542187
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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