A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360658



Internal ID21018211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:107200740..107234304hg38UCSC Ensembl
chr3:106919587..106953151hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg3833565
hg1933565
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18092669
Samples
Known GenesLINC00882
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360658
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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