A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18162417



Internal ID20729457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99411958..99414850hg38UCSC Ensembl
chr7:99009581..99012473hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg382893
hg192893
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6613451
Supporting Variants
Samples
Known GenesBUD31
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18162417
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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