A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18201869



Internal ID20768910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:235561244..235612758hg38UCSC Ensembl
chr1:235724544..235776058hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg3851515
hg1951515
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6330997
Supporting Variants
Samples
Known GenesGNG4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18201869
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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