A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18030076



Internal ID20597116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4073701..4108600hg38UCSC Ensembl
chr16:4123702..4158601hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3834900
hg1934900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6503064
Supporting Variants
Samples
Known GenesADCY9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18030076
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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