A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5622531



Internal ID21570836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:54077788..54077788hg38UCSC Ensembl
chrX:54104221..54104221hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg387443
hg197443
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17167679
SamplesHG02818
Known GenesFAM120C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5622531
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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