A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358204



Internal ID21015757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9992737..10046449hg38UCSC Ensembl
chr3:10034421..10088133hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3853713
hg1953713
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18105067
Samples
Known GenesCIDECP, EMC3-AS1, FANCD2, LOC401052
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358204
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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