A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6434129



Internal ID21091682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:138215122..138228631hg38UCSC Ensembl
chr7:137899868..137913377hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3813510
hg1913510
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155186
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6434129
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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