A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5666610



Internal ID21614915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154780559..154780755hg38UCSC Ensembl
chrX:154008834..154009030hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38197
hg19197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17166299
SamplesHG03486
Known GenesMPP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5666610
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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