A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844299



Internal ID22619234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:137862464..137870270hg38UCSC Ensembl
chr6:138183601..138191407hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg387807
hg197807
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501761
Samples
Known GenesLOC100130476, TNFAIP3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844299
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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