A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349482



Internal ID21007035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:68835992..68838221hg38UCSC Ensembl
chr2:69063124..69065353hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg382230
hg192230
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18088863
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349482
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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