A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570431



Internal ID20943502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:152288109..152582625hg38UCSC Ensembl
chr5:151667670..151962186hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg38294517
hg19294517
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268730
Samples
Known GenesNMUR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570431
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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