A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607887



Internal ID20980958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107374001..107377300hg38UCSC Ensembl
chr7:107014446..107017745hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18146961
Samples
Known GenesCOG5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607887
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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