A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335824



Internal ID20993377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:102205474..102257307hg38UCSC Ensembl
chr2:102821934..102873767hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg3851834
hg1951834
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205781
Samples
Known GenesIL1RL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335824
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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