A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111793



Internal ID22021027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:88705328..88802858hg38UCSC Ensembl
chrX:87960329..88057859hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg3897531
hg1997531
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17640594
Samples
Known GenesCPXCR1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111793
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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