A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17640827



Internal ID21832874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:44678596..44678725hg38UCSC Ensembl
chrX:44537842..44537971hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6104764
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17640827
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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