A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741763



Internal ID165429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:102851453..102851461hg38UCSC Ensembl
chrX:102106381..102106389hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5543634
Supporting Variants
Samples
Known GenesLINC00630
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741763
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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