A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423038



Internal ID21080591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:138700649..138705166hg38UCSC Ensembl
chr7:138385394..138389911hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg384518
hg194518
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155227
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423038
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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