A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352306



Internal ID21009859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:112726138..112736943hg38UCSC Ensembl
chr2:113483715..113494520hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg3810806
hg1910806
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18075579
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352306
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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