A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6040865



Internal ID21950203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:118386466..118386466hg38UCSC Ensembl
chrX:117520429..117520429hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg382983
hg192983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17640509
Samples
Known GenesMIR1277, WDR44
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6040865
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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