A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5672506



Internal ID21620811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3691430..3691484hg38UCSC Ensembl
chrX:3609471..3609525hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17167544
SamplesHG00732
Known GenesPRKX
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5672506
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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