A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496186



Internal ID20869385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67815575..67817266hg38UCSC Ensembl
chr16:67849478..67851169hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg381692
hg191692
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18030836
Samples
Known GenesTSNAXIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496186
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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