A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6353078



Internal ID21010631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:139252066..139260270hg38UCSC Ensembl
chr2:140009636..140017840hg19UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg388205
hg198205
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206612
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6353078
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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