A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361871



Internal ID21019424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:157335230..157516947hg38UCSC Ensembl
chr3:157053019..157234736hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg38181718
hg19181718
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210364
Samples
Known GenesPTX3, VEPH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361871
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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