A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498859



Internal ID20872073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4366505..4400037hg38UCSC Ensembl
chr16:4416506..4450038hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3833533
hg1933533
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183945
Samples
Known GenesCORO7, CORO7-PAM16, VASN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498859
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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