A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737653



Internal ID161319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:142756956..142774054hg38UCSC Ensembl
chrX:141844742..141861840hg19UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg3817099
hg1917099
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5416945
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737653
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00312175


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