A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335826



Internal ID20993379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:29051958..29058137hg38UCSC Ensembl
chr2:29274824..29281003hg19UCSC Ensembl
Cytoband2p23.2
Allele length
AssemblyAllele length
hg386180
hg196180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18088150
Samples
Known GenesFAM179A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335826
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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