A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6340802



Internal ID20998355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:200974401..200977100hg38UCSC Ensembl
chr2:201839124..201841823hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18084007
Samples
Known GenesFAM126B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6340802
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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