A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1070571



Internal ID18978178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:132143854..132144255hg38UCSC Ensembl
chr12:132628399..132628800hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771218
SamplesKWP1
Known GenesDDX51
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1070571
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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