A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421719



Internal ID21079272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140767405..140770007hg38UCSC Ensembl
chr7:140467205..140469807hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg382603
hg192603
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223280
Samples
Known GenesBRAF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421719
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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