A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742764



Internal ID166430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:141896200..141904600hg38UCSC Ensembl
chrX:140983986..140992386hg19UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg388401
hg198401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138624
Supporting Variants
Samples
Known GenesMAGEC1, MAGEC3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742764
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00292826


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