A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3999976



Internal ID19194666
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 StatusS
Merged Variantsnsv1147203
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3999976
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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