A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17648407



Internal ID21840454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:134959712..134959712hg38UCSC Ensembl
chrX:134093742..134093742hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38345
hg19345
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6053801
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17648407
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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