A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18165850



Internal ID20732890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30496256..30497631hg38UCSC Ensembl
chr8:30353773..30355148hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg381376
hg191376
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6426707
Supporting Variants
Samples
Known GenesRBPMS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18165850
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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