A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17645736



Internal ID21837783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:136918314..136918562hg38UCSC Ensembl
chrX:136000473..136000721hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38249
hg19249
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6107908
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17645736
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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