A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540764



Internal ID20914054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:100392424..100393180hg38UCSC Ensembl
chr3:100111268..100112024hg19UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg38757
hg19757
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18258868
Samples
Known GenesTOMM70A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540764
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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