A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209510



Internal ID20776550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:108736340..108741300hg38UCSC Ensembl
chr4:109657496..109662456hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg384961
hg194961
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6393173
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209510
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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