A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363196



Internal ID21020749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:78113892..78115664hg38UCSC Ensembl
chr3:78163043..78164815hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg381773
hg191773
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18105245
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363196
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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