A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17649319



Internal ID21841366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:38561445..38561521hg38UCSC Ensembl
chrX:38420698..38420774hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6107490
Supporting Variants
Samples
Known GenesTSPAN7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17649319
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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