A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1078385



Internal ID18974657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84219147..84220548hg38UCSC Ensembl
chr15:84887899..84889300hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg381402
hg191402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3767100
SamplesKWP1
Known GenesLOC388152
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1078385
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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