A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv954499



Internal ID17303373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:158570112..158573711hg38UCSC Ensembl
Outerchr3:158287901..158291500hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg383600
hg193600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001489
SamplesBILGI_BIOE
Known GenesLOC100996447, MLF1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv954499
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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