A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506407



Internal ID20879686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75936965..76008798hg38UCSC Ensembl
chr16:75970863..76042696hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3871834
hg1971834
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2936n223
Supporting Variantsnssv18032757
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506407
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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