A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17361420



Internal ID22587089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:16064438..16064438hg38UCSC Ensembl
chr11:16085984..16085984hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5974954
Supporting Variants
Samples
Known GenesSOX6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17361420
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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