A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6318063



Internal ID20851154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:45764925..45945984hg38UCSC Ensembl
chr1:46230597..46411656hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38181060
hg19181060
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv179n223
Supporting Variantsnssv18201369
Samples
Known GenesMAST2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6318063
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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