A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6618108



Internal ID20991179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:52453945..52476157hg38UCSC Ensembl
chr7:52521641..52543853hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg3822213
hg1922213
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217625
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6618108
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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