A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5416556



Internal ID195777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:7570388..7813452hg38UCSC Ensembl
chrX:7488429..7781493hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38243065
hg19293065
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17739121
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5416556
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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