A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1078212



Internal ID19321207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:90923389..90923443hg38UCSC Ensembl
Outerchr15:91466619..91466673hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3762535
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1078212
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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