A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561006



Internal ID333995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155075445..155075889hg38UCSC Ensembl
chrX:154303720..154304164hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38445
hg19445
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738174
Samples
Known GenesBRCC3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561006
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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