A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6618511



Internal ID20991582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:49184709..49455744hg38UCSC Ensembl
chr7:49224305..49495340hg19UCSC Ensembl
Cytoband7p12.2
Allele length
AssemblyAllele length
hg38271036
hg19271036
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219385
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6618511
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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