A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509051



Internal ID20882357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68135666..68147927hg38UCSC Ensembl
chr16:68169569..68181830hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3812262
hg1912262
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18031685
Samples
Known GenesNFATC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509051
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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