A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1071104



Internal ID18971201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:89010116..89013117hg38UCSC Ensembl
chr1:89475799..89478800hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg383002
hg193002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771413
SamplesKWP1
Known GenesGBP3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1071104
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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