A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110222



Internal ID22019455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:48601777..48623412hg38UCSC Ensembl
chrX:48460165..48481800hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3821636
hg1921636
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17637983
Samples
Known GenesWDR13
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110222
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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