A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950292



Internal ID17299166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:194248012..194254711hg38UCSC Ensembl
Outerchr3:193965801..193972500hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg386700
hg196700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996584
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950292
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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