A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2790514



Internal ID21235852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9705975..9705975hg38UCSC Ensembl
chr11:9727522..9727522hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38418
hg19418
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13692552
Samples
Known GenesSWAP70
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2790514
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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