A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106013



Internal ID22015246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:140723231..140725503hg38UCSC Ensembl
chrX:139805396..139807668hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg382273
hg192273
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17638652
Samples
Known GenesLINC00632
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106013
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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