A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6044015



Internal ID21953306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:64220920..64220920hg38UCSC Ensembl
chrX:63440800..63440800hg19UCSC Ensembl
CytobandXq11.2
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17641165
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6044015
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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