A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111651



Internal ID22020884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:82768923..82769547hg38UCSC Ensembl
chrX:82023931..82024555hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38625
hg19625
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17638198
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111651
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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