A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422639



Internal ID21080192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140900967..141043981hg38UCSC Ensembl
chr7:140600767..140743781hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38143015
hg19143015
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235719
Samples
Known GenesBRAF, MRPS33
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422639
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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