A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177706



Internal ID20744746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126651572..128129487hg38UCSC Ensembl
chr11:126521467..127999382hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg381477916
hg191477916
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6459462
Supporting Variants
Samples
Known GenesKIRREL3, KIRREL3-AS2, KIRREL3-AS3, MIR3167
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177706
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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