A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1079018



Internal ID19320786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:205209642..205209903hg38UCSC Ensembl
chr1:205178770..205179031hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38262
hg19262
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3770114
SamplesKWP1
Known GenesDSTYK
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1079018
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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