A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6108364



Internal ID22017598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:120581946..120582011hg38UCSC Ensembl
chrX:119715801..119715866hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17645281
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6108364
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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