A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503595



Internal ID20876851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:13711562..13712344hg38UCSC Ensembl
chr16:13805419..13806201hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg38783
hg19783
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028425
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503595
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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