A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077810



Internal ID18971197
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 StatusM
Merged Variants
Supporting Variantsnssv3765979
SamplesKWP1
Known GenesLOC388152
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077810
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer