A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17644851



Internal ID21836898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:129849744..129849744hg38UCSC Ensembl
chrX:128983720..128983720hg19UCSC Ensembl
CytobandXq26.1
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6048326
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17644851
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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