A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953271



Internal ID16955458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:30222894..30229493hg38UCSC Ensembl
Outerchr19:30713801..30720400hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg386600
hg196600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999807
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953271
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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