A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1073962



Internal ID18977116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13231267..13231410hg38UCSC Ensembl
chr6:13231499..13231642hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3764786
SamplesKWP1
Known GenesPHACTR1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1073962
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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