A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737387



Internal ID161053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:120609878..120609929hg38UCSC Ensembl
chrX:119743733..119743784hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559048
Supporting Variants
Samples
Known GenesMCTS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737387
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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