A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17640869



Internal ID21832916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:132028673..132028673hg38UCSC Ensembl
chrX:131162701..131162701hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6058639
Supporting Variants
Samples
Known GenesMST4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17640869
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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