A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1069881



Internal ID19318929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:82882881..82888920hg38UCSC Ensembl
chr15:83551633..83557672hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg386040
hg196040
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3767230
SamplesKWP1
Known GenesHOMER2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1069881
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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