A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17166299



Internal ID21476612
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 StatusS
Merged Variantsnsv5666610
Supporting Variants
SamplesHG03486
Known GenesMPP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17166299
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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