A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950023



Internal ID17298897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:186124912..186128211hg38UCSC Ensembl
Outerchr3:185842701..185846000hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996570
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950023
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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