A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154143



Internal ID18851606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:77487622..77487742hg38UCSC Ensembl
Outerchr17:75483704..75483824hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003413
SamplesKWB1
Known GenesSEPT9
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1154143
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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