A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505269



Internal ID20878536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:9680451..9682382hg38UCSC Ensembl
chr16:9774308..9776239hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg381932
hg191932
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18033960
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505269
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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