A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435438



Internal ID21092991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:148470453..148476622hg38UCSC Ensembl
chr7:148167545..148173714hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg386170
hg196170
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225075
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435438
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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