A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538841



Internal ID20858837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:101583050..101583957hg38UCSC Ensembl
chr3:101301894..101302801hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg38908
hg19908
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259472
Samples
Known GenesPCNP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538841
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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