A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501749



Internal ID20874986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:13864001..13864700hg38UCSC Ensembl
chr16:13957858..13958557hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028435
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501749
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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