A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6337233



Internal ID20994786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:102205055..102205999hg38UCSC Ensembl
chr2:102821515..102822459hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg38945
hg19945
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18074485
Samples
Known GenesIL1RL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6337233
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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