A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18158569



Internal ID20725609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:64511801..64515100hg38UCSC Ensembl
chr7:63972179..63975478hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6618404
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18158569
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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