A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2819689



Internal ID21265027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:61409361..61409361hg38UCSC Ensembl
chr9:40552980..40552980hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13703235
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2819689
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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