A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6446056



Internal ID21103609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:42740574..42887602hg38UCSC Ensembl
chr10:43236022..43383050hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38147029
hg19147029
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195461
Samples
Known GenesBMS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6446056
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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