A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737002



Internal ID160668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:52774964..52785000hg38UCSC Ensembl
chrX:52804036..52814044hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3810037
hg1910009
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5422108
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737002
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00235395


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