A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604154



Internal ID20977225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:80887055..81366473hg38UCSC Ensembl
chr7:80516371..80995789hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38479419
hg19479419
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217741
Samples
Known GenesSEMA3C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604154
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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