A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204467



Internal ID20771507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:78569713..78621755hg38UCSC Ensembl
chr1:79035398..79087440hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3852043
hg1952043
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6316977
Supporting Variants
Samples
Known GenesIFI44L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204467
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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