A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17434468



Internal ID22492338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:132851324..132853702hg38UCSC Ensembl
chrX:131985352..131987730hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg382379
hg192379
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5871709
Supporting Variants
Samples
Known GenesHS6ST2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17434468
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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