A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4746567



Internal ID20522581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:112776430..112776604hg38UCSC Ensembl
chr2:113534007..113534181hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16295249
Samples
Known GenesIL1A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4746567
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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