A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514078



Internal ID20887429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:13581879..13591352hg38UCSC Ensembl
chr16:13675736..13685209hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg389474
hg199474
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028414
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514078
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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