A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6371785



Internal ID21029338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:181890137..181906155hg38UCSC Ensembl
chr3:181607925..181623943hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg3816019
hg1916019
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211538
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6371785
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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