A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1120125



Internal ID19271948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:176430726..176451811hg38UCSC Ensembl
Outerchr2:177295454..177316539hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg3821086
hg1921086
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3960880
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1120125
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