A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212372



Internal ID20779412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:75560951..75569921hg38UCSC Ensembl
chr4:76486161..76495131hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg388971
hg198971
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6380525
Supporting Variants
Samples
Known GenesC4orf26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212372
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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