A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17642357



Internal ID21834404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:636548..636712hg38UCSC Ensembl
chrX:597283..597447hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6106375
Supporting Variants
Samples
Known GenesSHOX
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17642357
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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