A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603374



Internal ID20976445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:13576714..13697530hg38UCSC Ensembl
chr7:13616339..13737155hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38120817
hg19120817
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224867
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603374
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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