A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736683



Internal ID160349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:44790745..44791384hg38UCSC Ensembl
chrX:44649991..44650630hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38640
hg19640
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5425797
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736683
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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