A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5605732



Internal ID21554037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:54536221..54536221hg38UCSC Ensembl
chrX:54562654..54562654hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17167688
SamplesHG02818
Known GenesGNL3L
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5605732
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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