A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737495



Internal ID161161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:123789012..123789012hg38UCSC Ensembl
chrX:122922862..122922862hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg381899
hg191899
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560991
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737495
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0479326


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