A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955416



Internal ID16957603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:67731261..67731514hg38UCSC Ensembl
Outerchr17:65727377..65727630hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38254
hg19254
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001531
SamplesBILGI_BIOE
Known GenesNOL11
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955416
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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