A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868256



Internal ID22643191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:112530783..112536273hg38UCSC Ensembl
chrX:111774011..111779501hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg385491
hg195491
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17432187
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868256
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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