A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437406



Internal ID21094959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:41775201..41854300hg38UCSC Ensembl
chr10:42385909..42465008hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3879100
hg1979100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv699n223
Supporting Variantsnssv18184469
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437406
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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