A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737584



Internal ID161250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:130579211..130579211hg38UCSC Ensembl
chrX:129713185..129713185hg19UCSC Ensembl
CytobandXq26.1
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5537390
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737584
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000249626


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