A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505236



Internal ID20878503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:29067828..29077366hg38UCSC Ensembl
chr16:29079149..29088687hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg389539
hg199539
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029073
Samples
Known GenesRRN3P2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505236
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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