A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606020



Internal ID20979091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:114926162..114973486hg38UCSC Ensembl
chr7:114566217..114613541hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3847325
hg1947325
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233396
Samples
Known GenesMDFIC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606020
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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