A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2794619



Internal ID21239957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69300573..69300699hg38UCSC Ensembl
chr15:69592912..69593038hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13687806
Samples
Known GenesPAQR5
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2794619
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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