A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17457444



Internal ID22515326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:96373845..96375716hg38UCSC Ensembl
chrX:95628844..95630715hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg381872
hg191872
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5876039
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17457444
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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