A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1069025



Internal ID18972968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15719774..15719834hg38UCSC Ensembl
chr10:15761773..15761833hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3772169
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1069025
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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