A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6100901



Internal ID22010134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:34933301..35381606hg38UCSC Ensembl
chrX:34951418..35399723hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38448306
hg19448306
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17640137
Samples
Known GenesFAM47B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6100901
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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