A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6348739



Internal ID21006292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:102203501..102205300hg38UCSC Ensembl
chr2:102819961..102821760hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18074484
Samples
Known GenesIL1RL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6348739
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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