A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4001395



Internal ID19192121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:32444301..32446902hg38UCSC Ensembl
Outerchr9:32444299..32446900hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg382602
hg192602
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1153476
Supporting Variants
SamplesKWB1
Known GenesACO1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4001395
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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