A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739330



Internal ID162996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:13713974..13714024hg38UCSC Ensembl
chrX:13732093..13732143hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5538060
Supporting Variants
Samples
Known GenesTRAPPC2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739330
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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