A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101869



Internal ID22011102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:109556810..109556897hg38UCSC Ensembl
chrX:108800039..108800126hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641008
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101869
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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