A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110033



Internal ID22019266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:123130980..123288581hg38UCSC Ensembl
chrX:122264833..122422432hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38157602
hg19157600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17647338
Samples
Known GenesGRIA3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110033
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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