A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449891



Internal ID21107444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9622379..10132538hg38UCSC Ensembl
chr11:9643926..10154085hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38510160
hg19510160
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv975n223
Supporting Variantsnssv18194575
Samples
Known GenesLOC440028, SBF2, SBF2-AS1, SWAP70
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449891
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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