A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2814594



Internal ID21259932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63688231..63688231hg38UCSC Ensembl
chr6:64398132..64398132hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13704651
Samples
Known GenesPHF3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2814594
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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