A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506584



Internal ID20879866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:31164196..31167036hg38UCSC Ensembl
chr16:31175517..31178357hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg382841
hg192841
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028935
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506584
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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