A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106919



Internal ID22016152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:151703871..151703928hg38UCSC Ensembl
chrX:150872343..150872400hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17649172
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106919
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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