A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101504



Internal ID22010737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:57932056..57932492hg38UCSC Ensembl
chrX:57958490..57958926hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg38437
hg19437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17649335
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101504
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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