A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236270



Internal ID20803310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:87567555..87576912hg38UCSC Ensembl
chr8:88579783..88589140hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg389358
hg199358
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6428282
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236270
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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