A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6344977



Internal ID21002530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:102223294..102227643hg38UCSC Ensembl
chr2:102839754..102844103hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg384350
hg194350
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18075090
Samples
Known GenesIL1RL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6344977
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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