A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512368



Internal ID20885702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23208178..23208574hg38UCSC Ensembl
chr16:23219499..23219895hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38397
hg19397
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028785
Samples
Known GenesSCNN1G
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512368
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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