A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6344150



Internal ID21001703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:113010465..113106661hg38UCSC Ensembl
chr2:113768042..113864238hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg3896197
hg1996197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18075626
Samples
Known GenesIL1F10, IL36B, IL36RN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6344150
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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