A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510034



Internal ID20883348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:34188901..34214000hg38UCSC Ensembl
chr16:33991368..34016467hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3825100
hg1925100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2808n223
Supporting Variantsnssv18196670
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510034
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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