A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575517



Internal ID20948588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:179398330..179399261hg38UCSC Ensembl
chr3:179116118..179117049hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38932
hg19932
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263364
Samples
Known GenesGNB4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575517
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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