A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6107089



Internal ID22016322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:86625411..86862529hg38UCSC Ensembl
chrX:85880414..86117532hg19UCSC Ensembl
CytobandXq21.2
Allele length
AssemblyAllele length
hg38237119
hg19237119
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17642629
Samples
Known GenesDACH2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6107089
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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