A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209488



Internal ID20776528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:106361513..106476921hg38UCSC Ensembl
chr4:107282670..107398078hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38115409
hg19115409
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6376944
Supporting Variants
Samples
Known GenesGIMD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209488
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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