A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv954887



Internal ID17303760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:72731150..72739849hg38UCSC Ensembl
Outerchr3:72780301..72789000hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg388700
hg198700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001414
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv954887
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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