A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606623



Internal ID20979694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:69532585..69537266hg38UCSC Ensembl
chr7:68997571..69002252hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg384682
hg194682
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218249
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606623
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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