A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225011



Internal ID20792051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:4921507..4924240hg38UCSC Ensembl
chr6:4921741..4924474hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg382734
hg192734
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6411206
Supporting Variants
Samples
Known GenesCDYL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225011
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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