A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504424



Internal ID20877685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:26710106..26725284hg38UCSC Ensembl
chr16:26721427..26736605hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3815179
hg1915179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029235
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504424
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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