A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3978673



Internal ID18884606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:201837248..201837327hg38UCSC Ensembl
Outerchr1:201806376..201806455hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1116492
Supporting Variants
SamplesKWS2
Known GenesIPO9
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3978673
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