A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501844



Internal ID20875081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:65037007..65043047hg38UCSC Ensembl
chr16:65070910..65076950hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg386041
hg196041
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18031534
Samples
Known GenesCDH11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501844
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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