A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739258



Internal ID162924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:11610274..11610325hg38UCSC Ensembl
chrX:11628394..11628445hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38526
hg19526
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560612
Supporting Variants
Samples
Known GenesARHGAP6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739258
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.010675


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