A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1078895



Internal ID18970783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:2920319..2933121hg38UCSC Ensembl
chr3:2962003..2974805hg19UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg3812803
hg1912803
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3766894
SamplesKWP1
Known GenesCNTN4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1078895
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