A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360867



Internal ID21018420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:177685924..177705618hg38UCSC Ensembl
chr3:177403712..177423406hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3819695
hg1919695
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099725
Samples
Known GenesLINC00578
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360867
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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