A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443537



Internal ID21101090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9695662..9769837hg38UCSC Ensembl
chr11:9717209..9791384hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3874176
hg1974176
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195729
Samples
Known GenesLOC440028, SBF2-AS1, SWAP70
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443537
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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