A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741171



Internal ID164837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:85148000..85190542hg38UCSC Ensembl
chrX:84403006..84445548hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3842543
hg1942543
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6139062
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741171
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000627746


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