A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6046660



Internal ID21955893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:16183487..16183487hg38UCSC Ensembl
chrX:16201610..16201610hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17644150
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6046660
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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