A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737134



Internal ID160800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:103894542..103900542hg38UCSC Ensembl
chrX:103149463..103155463hg19UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg386001
hg196001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5423769
Supporting Variants
Samples
Known GenesMIR1256
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737134
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.17269


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