A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18170581



Internal ID20737621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:68301601..68304500hg38UCSC Ensembl
chr8:69213836..69216735hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg382900
hg192900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6420946
Supporting Variants
Samples
Known GenesLOC286189
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18170581
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00056


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