A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772697



Internal ID19306494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78677054..78683555hg38UCSC Ensembl
chr11:78388099..78394600hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg386502
hg196502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070056
Supporting Variants
SamplesKWP1
Known GenesTENM4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772697
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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