A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2819048



Internal ID21264386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:116289122..116289205hg38UCSC Ensembl
chr9:119051401..119051484hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv373n137
Supporting Variantsnssv13710949
Samples
Known GenesPAPPA
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2819048
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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