A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368520



Internal ID21026073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:177301359..177310458hg38UCSC Ensembl
chr3:177019147..177028246hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg389100
hg199100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099692
Samples
Known GenesLINC00501
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368520
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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