A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204455



Internal ID20771495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:77807699..77816866hg38UCSC Ensembl
chr1:78273384..78282551hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg389168
hg199168
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6331728
Supporting Variants
Samples
Known GenesFAM73A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204455
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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