A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6371622



Internal ID21029175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:57683388..57684935hg38UCSC Ensembl
chr3:57669115..57670662hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg381548
hg191548
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212282
Samples
Known GenesDENND6A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6371622
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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