A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6046442



Internal ID21955686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:13908982..13908982hg38UCSC Ensembl
chrX:13927101..13927101hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17645785
Samples
Known GenesGPM6B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6046442
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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