A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6104973



Internal ID22014207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:116821211..116896863hg38UCSC Ensembl
chrX:115955179..116030831hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3875653
hg1975653
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641616
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6104973
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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