A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6046504



Internal ID21955743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:85283777..85283777hg38UCSC Ensembl
chrX:84538783..84538783hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg381745
hg191745
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639764
Samples
Known GenesPOF1B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6046504
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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