A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150529



Internal ID18852783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:74346427..74346485hg38UCSC Ensembl
Outerchr9:76961343..76961401hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3996003
SamplesKWB1
Known GenesMIR6130
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150529
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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