A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219659



Internal ID20786699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:4492785..4518410hg38UCSC Ensembl
chr6:4493019..4518644hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3825626
hg1925626
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6409573
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219659
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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