A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111172



Internal ID22020405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:40885250..40885354hg38UCSC Ensembl
chrX:40744503..40744607hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17638286
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111172
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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