A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953839



Internal ID16956026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:18089487..18146586hg38UCSC Ensembl
Outerchr17:17992801..18049900hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3857100
hg1957100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000257
SamplesBILGI_BIOE
Known GenesDRG2, MYO15A
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953839
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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