A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077809



Internal ID18972353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84207047..84213748hg38UCSC Ensembl
chr15:84875799..84882500hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg386702
hg196702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3766800
SamplesKWP1
Known GenesLOC388152, LOC440300
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077809
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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