A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3770171



Internal ID19311118
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 StatusS
Merged Variantsnsv1079028
Supporting Variants
SamplesKWP1
Known GenesACSM2A, ACSM2B, ACSM5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3770171
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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