A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2795238



Internal ID21240576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41293511..41293578hg38UCSC Ensembl
chr15:41585709..41585776hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13684248
Samples
Known GenesOIP5-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2795238
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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