A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6104697



Internal ID22013930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:6421214..6424061hg38UCSC Ensembl
chrX:6339255..6342102hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg382848
hg192848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641889
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6104697
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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