A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17643181



Internal ID21835228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:44443842..44446852hg38UCSC Ensembl
chrX:44303088..44306098hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg383011
hg193011
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6112633
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17643181
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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