A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4734581



Internal ID20510518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:113130540..113130712hg38UCSC Ensembl
chr2:113888117..113888289hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg38173
hg19173
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16284912
Samples
Known GenesIL1RN
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4734581
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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