A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17073748



Internal ID21489935
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 Variantsnsv5658667
Supporting Variants
SamplesNA19238
Known GenesSOX6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17073748
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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