A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17644452



Internal ID21836499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:41363669..41363746hg38UCSC Ensembl
chrX:41222922..41222999hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6101875
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17644452
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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