A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5431226



Internal ID210009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155074479..155075251hg38UCSC Ensembl
chrX:154302754..154303526hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38773
hg19773
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738170
Samples
Known GenesBRCC3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5431226
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer