A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18121443



Internal ID20688483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:96863901..96870600hg38UCSC Ensembl
chr4:97785052..97791751hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg386700
hg196700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6379826
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18121443
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00756


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