A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541642



Internal ID20914924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:42609010..42610187hg38UCSC Ensembl
chr3:42650502..42651679hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg381178
hg191178
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4855n223
Supporting Variantsnssv18260683
Samples
Known GenesNKTR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541642
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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