A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354261



Internal ID21011814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:102200557..102208688hg38UCSC Ensembl
chr2:102817017..102825148hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg388132
hg198132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18074483
Samples
Known GenesIL1RL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354261
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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