A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616950



Internal ID20990021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:79842901..79853000hg38UCSC Ensembl
chr7:79472217..79482316hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3810100
hg1910100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6973n223
Supporting Variantsnssv18229223
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616950
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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