A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6040704



Internal ID21950043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:66622487..66622487hg38UCSC Ensembl
chrX:65842329..65842329hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17638410
Samples
Known GenesEDA2R
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6040704
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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