A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504895



Internal ID20878159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19230400..19231523hg38UCSC Ensembl
chr16:19241722..19242845hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg381124
hg191124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028137
Samples
Known GenesSYT17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504895
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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