A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508269



Internal ID20881568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12329867..12364279hg38UCSC Ensembl
chr16:12423724..12458136hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3834413
hg1934413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028690
Samples
Known GenesSNX29
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508269
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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