A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2817364



Internal ID21262702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:134992439..134992439hg38UCSC Ensembl
chr9:137884285..137884285hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38286
hg19286
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13699835
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2817364
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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