A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2817749



Internal ID21263087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:54059290..54059603hg38UCSC Ensembl
chr8:54971850..54972163hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13698563
Samples
Known GenesLYPLA1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2817749
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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