A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17640594



Internal ID21832641
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 StatusS
Merged Variantsnsv6111793
Supporting Variants
Samples
Known GenesCPXCR1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17640594
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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