A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515559



Internal ID20888919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:7751424..7820420hg38UCSC Ensembl
chr16:7801426..7870422hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3868997
hg1968997
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191718
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515559
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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