A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498681



Internal ID20871894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:76608706..77690545hg38UCSC Ensembl
chr16:76642603..77724442hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg381081840
hg191081840
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195300
Samples
Known GenesADAMTS18, MIR4719, MON1B, SYCE1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498681
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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