A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601133



Internal ID20974204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:106905656..106911626hg38UCSC Ensembl
chr7:106546101..106552071hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg385971
hg195971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18149506
Samples
Known GenesPIK3CG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601133
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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