A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366219



Internal ID21023772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:56289517..56290116hg38UCSC Ensembl
chr3:56323545..56324144hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18102824
Samples
Known GenesERC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366219
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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