A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742683



Internal ID166349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:140396229..140406658hg38UCSC Ensembl
chrX:139478394..139488823hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg3810430
hg1910430
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5427541
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742683
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00270552


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