A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367303



Internal ID21024856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:177663501..177666600hg38UCSC Ensembl
chr3:177381289..177384388hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg383100
hg193100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5105n223
Supporting Variantsnssv18099723
Samples
Known GenesLINC00578
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367303
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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