A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17452122



Internal ID22509994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:4578538..4578700hg38UCSC Ensembl
chrX:4496579..4496741hg19UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg38163
hg19163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5881289
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17452122
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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