A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4434898



Internal ID21396900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:26019773..26056772hg38UCSC Ensembl
chr6:26020001..26057000hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3837000
hg1937000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15752957
SamplesSMI041
Known GenesHIST1H1C, HIST1H2AB, HIST1H2BB, HIST1H3A, HIST1H3B, HIST1H3C, HIST1H4A, HIST1H4B
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4434898
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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