A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367181



Internal ID21024734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:157305273..157312921hg38UCSC Ensembl
chr3:157023062..157030710hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg387649
hg197649
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210363
Samples
Known GenesVEPH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367181
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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