A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738149



Internal ID161815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154781326..154781426hg38UCSC Ensembl
chrX:154009601..154009701hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5428022
Supporting Variants
Samples
Known GenesMPP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738149
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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