A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18116315



Internal ID20683355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39643224..39647997hg38UCSC Ensembl
chr4:39644844..39649617hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg384774
hg194774
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6387112
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18116315
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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