A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6337029



Internal ID20994582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:104212902..104221225hg38UCSC Ensembl
chr2:104829360..104837683hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg388324
hg198324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18076583
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6337029
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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