A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17457130



Internal ID22515011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:53112594..53115586hg38UCSC Ensembl
chrX:53141776..53144768hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg382993
hg192993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5877794
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17457130
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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