A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111460



Internal ID22020694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:75173292..75173368hg38UCSC Ensembl
chrX:74393127..74393203hg19UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17644816
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111460
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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