A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1147741



Internal ID18851377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:74301916..74302101hg38UCSC Ensembl
Outerchr17:72298055..72298240hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38186
hg19186
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3996525
SamplesKWB1
Known GenesDNAI2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1147741
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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