A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224298



Internal ID20791338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:88025328..88043359hg38UCSC Ensembl
chr8:89037556..89055587hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3818032
hg1918032
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6417109
Supporting Variants
Samples
Known GenesMMP16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224298
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00054


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