A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105888



Internal ID22015121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:42952580..42952756hg38UCSC Ensembl
chrX:42811829..42812005hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641463
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105888
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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