A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424832



Internal ID21082385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:154599601..154634400hg38UCSC Ensembl
chr7:154391311..154426110hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3834800
hg1934800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220481
Samples
Known GenesDPP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424832
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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