A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1074954



Internal ID19321771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:111872196..111873197hg38UCSC Ensembl
chr6:112193399..112194400hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381002
hg191002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3766550
SamplesKWP1
Known GenesFYN
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1074954
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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