A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17465589



Internal ID22523478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:5155235..5156152hg38UCSC Ensembl
chrX:5073276..5074193hg19UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg38918
hg19918
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5884405
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17465589
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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