A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6107915



Internal ID22017150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:41361385..41361454hg38UCSC Ensembl
chrX:41220638..41220707hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17646845
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6107915
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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