A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349069



Internal ID21006622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:38540362..38540872hg38UCSC Ensembl
chr2:38767504..38768014hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg38511
hg19511
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18086365
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349069
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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