A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2790571



Internal ID21235909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101925705..101925705hg38UCSC Ensembl
chr11:101796436..101796436hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38816
hg19816
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13688452, nssv13694422
Samples
Known GenesKIAA1377
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2790571
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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