A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105685



Internal ID22014918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:144477628..144506330hg38UCSC Ensembl
chrX:143559192..143587869hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg3828703
hg1928678
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17645105
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105685
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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