A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5606510



Internal ID21554815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:15401360..15401360hg38UCSC Ensembl
chrX:15419482..15419482hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17166122
SamplesHG00732
Known GenesPIR, PIR-FIGF
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5606510
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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