A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6344862



Internal ID21002415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:234695140..234695922hg38UCSC Ensembl
chr2:235603784..235604566hg19UCSC Ensembl
Cytoband2q37.2
Allele length
AssemblyAllele length
hg38783
hg19783
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18087365
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6344862
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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