A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110972



Internal ID22020205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:4974512..5181552hg38UCSC Ensembl
chrX:4892553..5099593hg19UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg38207041
hg19207041
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17643213
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110972
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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