A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2434



Internal ID15540697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:184436274..184467716hg38UCSC Ensembl
Outerchr3:184154062..184185504hg19UCSC Ensembl
Outerchr3:185636756..185668198hg18UCSC Ensembl
Outerchr3:185636764..185668206hg17UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg388588
hg198588
hg188588
hg178588
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4147
Supporting Variants
SamplesNA18555
Known Genes
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv2434
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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