A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737506



Internal ID161172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:123909623..123909674hg38UCSC Ensembl
chrX:123043473..123043524hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5562762
Supporting Variants
Samples
Known GenesXIAP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737506
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002185


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