A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609852



Internal ID20982923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:87871601..87876900hg38UCSC Ensembl
chr7:87500916..87506215hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg385300
hg195300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236493
Samples
Known GenesDBF4, SLC25A40
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609852
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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