A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418083



Internal ID21075636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:145732783..145733486hg38UCSC Ensembl
chr7:145429876..145430579hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38704
hg19704
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155730
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418083
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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