A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6102778



Internal ID22012012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:115960285..115960447hg38UCSC Ensembl
chrX:115076618..115076780hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38163
hg19163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17649322
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6102778
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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