A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737835



Internal ID161501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:147365272..147365272hg38UCSC Ensembl
chrX:146446790..146446790hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg38585
hg19585
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5547806
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737835
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000249626


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