A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765979



Internal ID18966184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84222347..84223648hg38UCSC Ensembl
chr15:84891099..84892400hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg381302
hg191302
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1077810
Supporting Variants
SamplesKWP1
Known GenesLOC388152
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765979
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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