A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6336880



Internal ID20994433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:201380208..201382839hg38UCSC Ensembl
chr2:202244931..202247562hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg382632
hg192632
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18084586
Samples
Known GenesTRAK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6336880
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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