A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1079028



Internal ID19321220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:20432220..20591666hg38UCSC Ensembl
chr16:20443542..20602988hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38159447
hg19159447
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3770171
SamplesKWP1
Known GenesACSM2A, ACSM2B, ACSM5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1079028
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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