A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178300



Internal ID20745340
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 StatusS
Merged Variantsnsv6463092
Supporting Variants
Samples
Known GenesINTS4, KCTD14, NDUFC2, NDUFC2-KCTD14, RNU6-83P, THRSP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178300
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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