A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953242



Internal ID17302116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:107313854..107321453hg38UCSC Ensembl
Outerchr3:107032701..107040300hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg387600
hg197600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001439
SamplesBILGI_BIOE
Known GenesLINC00883
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953242
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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