A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17740757



Internal ID164423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:74247753..74247804hg38UCSC Ensembl
chrX:73467588..73467639hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5561782
Supporting Variants
Samples
Known GenesFTX
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17740757
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000781


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