A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741934



Internal ID165600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:109727330..109727381hg38UCSC Ensembl
chrX:108970559..108970610hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5558664
Supporting Variants
Samples
Known GenesACSL4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741934
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000625


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