A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6618010



Internal ID20991081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:137866801..137867300hg38UCSC Ensembl
chr6:138187938..138188437hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18138366
Samples
Known GenesLOC100130476, TNFAIP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6618010
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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