A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv373n137



Internal ID22812993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:116289122..116289221hg38UCSC Ensembl
chr9:119051401..119051500hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv2819049, nsv2819048
Samples
Known GenesPAPPA
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)dgv373n137
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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