A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419106



Internal ID21076659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:133376370..134327385hg38UCSC Ensembl
chr7:133061124..134012137hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38951016
hg19951014
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228713
Samples
Known GenesEXOC4, LRGUK, SLC35B4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419106
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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