A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426680



Internal ID21084233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:143727001..143743200hg38UCSC Ensembl
chr7:143424094..143440293hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3816200
hg1916200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230898
Samples
Known GenesFAM115C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426680
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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