A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368404



Internal ID21025957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:107045976..107046630hg38UCSC Ensembl
chr3:106764823..106765477hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg38655
hg19655
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18092658
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368404
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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