A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1069044



Internal ID18973375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:94773951..94774239hg38UCSC Ensembl
chr10:47088411..47088699hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3769456
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1069044
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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