A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6049112



Internal ID21958345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:16714706..16714706hg38UCSC Ensembl
chrX:16732829..16732829hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17646944
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6049112
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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