A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463092



Internal ID21120645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77925634..78075013hg38UCSC Ensembl
chr11:77636680..77786059hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38149380
hg19149380
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178300
Samples
Known GenesINTS4, KCTD14, NDUFC2, NDUFC2-KCTD14, RNU6-83P, THRSP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463092
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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