A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329621



Internal ID20862774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:45697504..45964189hg38UCSC Ensembl
chr1:46163176..46429861hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38266686
hg19266686
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv178n223
Supporting Variantsnssv18201365
Samples
Known GenesIPP, MAST2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329621
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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