A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3996003



Internal ID18844076
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 StatusS
Merged Variantsnsv1150529
Supporting Variants
SamplesKWB1
Known GenesMIR6130
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3996003
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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