A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498518



Internal ID20871729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75013433..75051604hg38UCSC Ensembl
chr16:75047331..75085502hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3838172
hg1938172
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190013
Samples
Known GenesZNRF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498518
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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