A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508705



Internal ID20882009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10696801..10698800hg38UCSC Ensembl
chr16:10790658..10792657hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2688n223
Supporting Variantsnssv18028295
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508705
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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