A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359545



Internal ID21017098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:56310858..56316465hg38UCSC Ensembl
chr3:56344886..56350493hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg385608
hg195608
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18102825
Samples
Known GenesERC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359545
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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