A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1068707



Internal ID19318722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6312435..6328118hg38UCSC Ensembl
chr6:6312668..6328351hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3815684
hg1915684
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771233
SamplesKWP1
Known GenesF13A1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1068707
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer