A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354090



Internal ID21011643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:196957244..196964258hg38UCSC Ensembl
chr2:197821968..197828982hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg387015
hg197015
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18083648
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354090
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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