A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737936



Internal ID161602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:150072700..150097033hg38UCSC Ensembl
chrX:149240931..149265264hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3824334
hg1924334
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5428106
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737936
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000416233


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