A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5425627



Internal ID204584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155071051..155217414hg38UCSC Ensembl
chrX:154299326..154445691hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38146364
hg19146366
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738169
Samples
Known GenesBRCC3, CMC4, MTCP1, VBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5425627
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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