A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608997



Internal ID20982068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:46956065..47010614hg38UCSC Ensembl
chr7:46995663..47050212hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg3854550
hg1954550
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218783
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608997
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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