A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772006



Internal ID19305284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89213898..89214212hg38UCSC Ensembl
chr6:89923617..89923931hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1068318
Supporting Variants
SamplesKWP1
Known GenesGABRR1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772006
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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