A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6345537



Internal ID21003090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:215546901..215553500hg38UCSC Ensembl
chr2:216411624..216418223hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg386600
hg196600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18084040
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6345537
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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