A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738136



Internal ID161802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154569606..154583606hg38UCSC Ensembl
chrX:153797837..153811870hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3814001
hg1914034
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5420027
Supporting Variants
Samples
Known GenesFAM223A, FAM223B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738136
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000670092


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