A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1116450



Internal ID18931636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:4940878..5021264hg38UCSC Ensembl
Outerchr10:4983070..5063456hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3880387
hg1980387
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv348n106
Supporting Variantsnssv3978631
SamplesKWS2
Known GenesAKR1C1, AKR1C2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1116450
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