A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419026



Internal ID21076579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128746276..128746905hg38UCSC Ensembl
chr7:128386330..128386959hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg38630
hg19630
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236979
Samples
Known GenesCALU
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419026
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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