A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6340719



Internal ID20998272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:165874701..165876100hg38UCSC Ensembl
chr2:166731211..166732610hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18081256
Samples
Known GenesTTC21B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6340719
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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