A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1069051



Internal ID18972841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45876167..45959937hg38UCSC Ensembl
chr10:51635899..51723000hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3883771
hg1987102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3767719
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1069051
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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