A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109606



Internal ID22018839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:44445728..44446002hg38UCSC Ensembl
chrX:44304974..44305248hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38275
hg19275
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17647776
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109606
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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