A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6042530



Internal ID21951846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:35692247..35692247hg38UCSC Ensembl
chrX:35710364..35710364hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17646963
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6042530
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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