A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444581



Internal ID21102134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9622154..10132457hg38UCSC Ensembl
chr11:9643701..10154004hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38510304
hg19510304
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv975n223
Supporting Variantsnssv18177243
Samples
Known GenesLOC440028, SBF2, SBF2-AS1, SWAP70
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444581
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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