A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186230



Internal ID20753271
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 StatusS
Merged Variantsnsv6459128
Supporting Variants
Samples
Known GenesACY3, ALDH3B2, DOC2GP, FAM86C2P, GSTP1, NDUFV1, NUDT8, TBX10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186230
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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