A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608712



Internal ID20981783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107578601..107580900hg38UCSC Ensembl
chr7:107219046..107221345hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224230
Samples
Known GenesBCAP29
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608712
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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