A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953947



Internal ID16956134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:3148003..3156702hg38UCSC Ensembl
Outerchr19:3148001..3156700hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg388700
hg198700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998926
SamplesBILGI_BIOE
Known GenesGNA15
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953947
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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