A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498033



Internal ID20871241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:30815043..30831621hg38UCSC Ensembl
chr16:30826364..30842942hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3816579
hg1916579
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029188
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498033
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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