A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737441



Internal ID161107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:122480158..122492691hg38UCSC Ensembl
chrX:121614011..121626544hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3812534
hg1912534
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138636
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737441
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000832466


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