A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18108756



Internal ID20675796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:141672535..141673084hg38UCSC Ensembl
chr4:142593688..142594237hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38550
hg19550
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6375943
Supporting Variants
Samples
Known GenesIL15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18108756
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00092


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