A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18173088



Internal ID20740128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:89937432..89938183hg38UCSC Ensembl
chr8:90949660..90950411hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38752
hg19752
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6428585
Supporting Variants
Samples
Known GenesNBN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18173088
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00042


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