A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1069770



Internal ID18977297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:108214651..108215552hg38UCSC Ensembl
chr13:108866999..108867900hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38902
hg19902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3762350
SamplesKWP1
Known GenesLIG4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1069770
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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