A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5605942



Internal ID21554247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:84214069..84214069hg38UCSC Ensembl
chrX:83469077..83469077hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38217
hg19217
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17168695
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5605942
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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