A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6112534



Internal ID22021767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:21763490..21785360hg38UCSC Ensembl
chrX:21781608..21803478hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg3821871
hg1921871
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641521
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6112534
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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