A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18162283



Internal ID20729323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:105438401..105440500hg38UCSC Ensembl
chr8:106450629..106452728hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6417150
Supporting Variants
Samples
Known GenesZFPM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18162283
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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