A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5415855



Internal ID195102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:49097451..49109871hg38UCSC Ensembl
chrX:48954391..48966809hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3812421
hg1912419
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736893
Samples
Known GenesWDR45
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5415855
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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