A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616902



Internal ID20989973
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 StatusM
Merged Variants
Supporting Variantsnssv18217426
Samples
Known GenesPHF14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616902
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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