A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111674



Internal ID22020907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:21987124..21987255hg38UCSC Ensembl
chrX:22005242..22005373hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641848
Samples
Known GenesSMS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111674
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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