A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv623642



Internal ID15475529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:21684122..21745832hg38UCSC Ensembl
Outerchr13:22258261..22319971hg19UCSC Ensembl
Outerchr13:21156261..21217971hg18UCSC Ensembl
Outerchr13:21156261..21217971hg17UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg383131
hg193131
hg183131
hg173131
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv509497
Supporting Variants
SamplesNA18994
Known GenesFGF9
MethodOptical mapping
AnalysisSingle-molecule optical maps were assembled into genome-wide consensus maps. These consensus maps were compared to a restriction map generated from the NCBI b35 human genome reference sequence.
PlatformOptical Mapping
Comments
ReferenceTeague_et_al_2010
Pubmed ID20534489
Accession Number(s)nssv623642
Frequency
Sample Size4
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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