A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217426



Internal ID20784466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:10985813..11271791hg38UCSC Ensembl
chr7:11025440..11311418hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38285979
hg19285979
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6616902
Supporting Variants
Samples
Known GenesPHF14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217426
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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