A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6055567



Internal ID21964800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:53967188..53967188hg38UCSC Ensembl
chrX:53993621..53993621hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17648893
Samples
Known GenesPHF8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6055567
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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