A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496604



Internal ID20869807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:63251001..63362500hg38UCSC Ensembl
chr16:63284905..63396404hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38111500
hg19111500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2904n223
Supporting Variantsnssv18196592
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496604
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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