A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18116359



Internal ID20683399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:41520761..41521355hg38UCSC Ensembl
chr4:41522778..41523372hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38595
hg19595
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6379430
Supporting Variants
Samples
Known GenesLIMCH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18116359
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00037


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