A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv954658



Internal ID16956845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:45023882..45024003hg38UCSC Ensembl
Outerchr19:45527140..45527261hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3002912
SamplesBILGI_BIOE
Known GenesRELB
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv954658
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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