A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3771271



Internal ID19304869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:12928173..12928255hg38UCSC Ensembl
chr12:13081107..13081189hg19UCSC Ensembl
Cytoband12p13.1
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1077769
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3771271
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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