A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203162



Internal ID20770202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:91542601..91547900hg38UCSC Ensembl
chr1:92008158..92013457hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg385300
hg195300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6323038
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203162
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0002


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