A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515179



Internal ID20888538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:8616322..8691646hg38UCSC Ensembl
chr16:8710179..8785503hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3875325
hg1975325
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196510
Samples
Known GenesABAT, METTL22
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515179
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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