A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349859



Internal ID21007412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:222479915..222484720hg38UCSC Ensembl
chr2:223344634..223349439hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg384806
hg194806
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18086933
Samples
Known GenesSGPP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349859
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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