A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18201659



Internal ID20768700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:170092701..170110700hg38UCSC Ensembl
chr1:170061842..170079841hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3818000
hg1918000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6315980
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18201659
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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