A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512104



Internal ID20885434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:8383072..8384080hg38UCSC Ensembl
chr16:8433074..8434082hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg381009
hg191009
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18032490
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512104
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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