A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5426753



Internal ID205675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:111555679..111559574hg38UCSC Ensembl
chrX:110798907..110802802hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg383896
hg193896
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741986
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5426753
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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