A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5606662



Internal ID21554967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:133435092..133435092hg38UCSC Ensembl
chrX:132569120..132569120hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg3816427
hg1916427
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17165312
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5606662
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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