A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6107908



Internal ID22017143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:136918314..136918562hg38UCSC Ensembl
chrX:136000473..136000721hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38249
hg19249
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17645736
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6107908
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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