A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1147203



Internal ID19198883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:123346620..123347921hg38UCSC Ensembl
Outerchr9:126108899..126110200hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg381302
hg191302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3999976
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1147203
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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