A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6353104



Internal ID21010657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:13491246..13592362hg38UCSC Ensembl
chr2:13631371..13732487hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38101117
hg19101117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18077630
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6353104
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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