A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1078888



Internal ID19318367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:23379882..23799897hg38UCSC Ensembl
chr19:23562684..23982699hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38420016
hg19420016
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3767855
SamplesKWP1
Known GenesRPSAP58, ZNF675, ZNF681, ZNF91
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1078888
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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