A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500661



Internal ID20873889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89839303..90017373hg38UCSC Ensembl
chr16:89905711..90083781hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38178071
hg19178071
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18033839
Samples
Known GenesAFG3L1P, CENPBD1, DBNDD1, DEF8, MC1R, SPIRE2, TCF25, TUBB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500661
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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