A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16288248



Internal ID20497466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:41443185..41443287hg38UCSC Ensembl
chr4:41445202..41445304hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4734615
Supporting Variants
Samples
Known GenesLIMCH1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16288248
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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