A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18170607



Internal ID20737647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:68658638..68659107hg38UCSC Ensembl
chr8:69570873..69571342hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg38470
hg19470
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6429454
Supporting Variants
Samples
Known GenesC8orf34
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18170607
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00026


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