A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6108425



Internal ID22017659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:85088812..85088864hg38UCSC Ensembl
chrX:84343818..84343870hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17640248
Samples
Known GenesAPOOL
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6108425
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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