A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18165862



Internal ID20732902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30700564..30702132hg38UCSC Ensembl
chr8:30558081..30559649hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg381569
hg191569
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6423140
Supporting Variants
Samples
Known GenesGSR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18165862
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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