A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3768987



Internal ID19308408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89507668..89508869hg38UCSC Ensembl
chr15:90050899..90052100hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381202
hg191202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070296
Supporting Variants
SamplesKWP1
Known GenesLINC00928
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3768987
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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