A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5624280



Internal ID21572585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:40211110..40211110hg38UCSC Ensembl
chrX:40070363..40070363hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17167064
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5624280
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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