A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101358



Internal ID22010591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:21674394..21674491hg38UCSC Ensembl
chrX:21692512..21692609hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641492
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101358
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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