A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418720



Internal ID21076273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142008064..142008771hg38UCSC Ensembl
chr7:141707864..141708571hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38708
hg19708
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221066
Samples
Known GenesMGAM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418720
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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