A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326630



Internal ID20859767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23517912..23518233hg38UCSC Ensembl
chr1:23844404..23844725hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202414
Samples
Known GenesE2F2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326630
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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