A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18168997



Internal ID20736037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39030893..39033691hg38UCSC Ensembl
chr8:38888412..38891210hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg382799
hg192799
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6427154
Supporting Variants
Samples
Known GenesADAM9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18168997
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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