A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110877



Internal ID18931134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:114103332..114111749hg38UCSC Ensembl
Outerchr1:114645954..114654371hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg388418
hg198418
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3961289
SamplesKWS1
Known GenesSYT6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110877
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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