A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2817864



Internal ID21263202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:41480492..41480492hg38UCSC Ensembl
chr9:42128881..42128881hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13700607
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2817864
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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