A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6340702



Internal ID20998255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:195616522..195617880hg38UCSC Ensembl
chr2:196481246..196482604hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg381359
hg191359
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18081911
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6340702
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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