A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5869759



Internal ID22644694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:115530663..115530891hg38UCSC Ensembl
chrX:114764990..114765218hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38229
hg19229
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17430187
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5869759
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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