A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367586



Internal ID21025139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:43453419..43459018hg38UCSC Ensembl
chr3:43494911..43500510hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg385600
hg195600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099963
Samples
Known GenesANO10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367586
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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