A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18145357



Internal ID20712397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89841195..89843843hg38UCSC Ensembl
chr6:90550914..90553562hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg382649
hg192649
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6412857
Supporting Variants
Samples
Known GenesCASP8AP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18145357
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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