A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17640898



Internal ID21832945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:123260495..123260495hg38UCSC Ensembl
chrX:122394346..122394346hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6050568
Supporting Variants
Samples
Known GenesGRIA3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17640898
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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