A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453605



Internal ID21111158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:8836740..9205220hg38UCSC Ensembl
chr11:8858287..9226767hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38368481
hg19368481
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187311
Samples
Known GenesAKIP1, ASCL3, C11orf16, DENND5A, KRT8P41, MIR5691, NRIP3, SCUBE2, ST5, TMEM9B, TMEM9B-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453605
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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