A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617253



Internal ID20990324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:15561885..15569608hg38UCSC Ensembl
chr7:15601510..15609233hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg387724
hg197724
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226834
Samples
Known GenesAGMO
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617253
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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