A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332337



Internal ID20865507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:818880..922257hg38UCSC Ensembl
chr1:754260..857637hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg38103378
hg19103378
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4n223
Supporting Variantsnssv18205126
Samples
Known GenesFAM41C, FAM87B, LINC00115, LINC01128, LOC100130417
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332337
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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