A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1148606



Internal ID19197591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:64413817..64493086hg38UCSC Ensembl
Outerchr9:43003799..43089300hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3879270
hg1985502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4000646
SamplesKWB1
Known GenesFAM95B1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1148606
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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