A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463048



Internal ID21120601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77702166..77945031hg38UCSC Ensembl
chr11:77413211..77656077hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38242866
hg19242867
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184066
Samples
Known GenesAAMDC, INTS4, RSF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463048
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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