A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2817892



Internal ID21263230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66696469..66696469hg38UCSC Ensembl
chr9:41825511..41825511hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13703888
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2817892
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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