A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5428156



Internal ID207035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:145992669..145994167hg38UCSC Ensembl
chrX:145074187..145075685hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg381499
hg191499
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17737758
Samples
Known GenesMIR892C
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5428156
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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