A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1150202



Internal ID18850763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:29540778..29543879hg38UCSC Ensembl
Outerchr16:29552099..29555200hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg383102
hg193102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003503
SamplesKWB1
Known GenesLOC440354
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1150202
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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