A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459128



Internal ID21116681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67577616..67989511hg38UCSC Ensembl
chr11:67345087..67756982hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38411896
hg19411896
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186230
Samples
Known GenesACY3, ALDH3B2, DOC2GP, FAM86C2P, GSTP1, NDUFV1, NUDT8, TBX10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459128
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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