A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950384



Internal ID16952571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:31571200..31588799hg38UCSC Ensembl
Outerchr1:32036801..32054400hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg3817600
hg1917600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997118
SamplesBILGI_BIOE
Known GenesTINAGL1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950384
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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