A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364296



Internal ID21021849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:56626537..56630772hg38UCSC Ensembl
chr3:56660565..56664800hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg384236
hg194236
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18102848
Samples
Known GenesFAM208A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364296
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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