A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16295679



Internal ID20504897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63688218..63688218hg38UCSC Ensembl
chr6:64398119..64398119hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4767030
Supporting Variants
Samples
Known GenesPHF3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16295679
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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