A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6053084



Internal ID21962318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:137431923..137431923hg38UCSC Ensembl
chrX:136514082..136514082hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17643673
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6053084
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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