A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105246



Internal ID22014479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:119769421..119769491hg38UCSC Ensembl
chrX:118903384..118903454hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17637731
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105246
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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