A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2795319



Internal ID21240657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92768723..92768802hg38UCSC Ensembl
chr15:93311953..93312032hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13692133
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2795319
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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