A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15745690



Internal ID21386108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131680107..131681106hg38UCSC Ensembl
chr11:131550001..131551000hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4431448
Supporting Variants
SamplesMDQ010
Known GenesNTM
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15745690
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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