A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407095



Internal ID21064648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:157136790..157140751hg38UCSC Ensembl
chr5:156563801..156567762hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg383962
hg193962
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215911
Samples
Known GenesMED7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407095
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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