A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515034



Internal ID20888390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68202582..68213555hg38UCSC Ensembl
chr16:68236485..68247458hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3810974
hg1910974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18031688
Samples
Known GenesNFATC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515034
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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