A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3785



Internal ID15548429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:43185987..43220168hg38UCSC Ensembl
Outerchr3:43227479..43261660hg19UCSC Ensembl
Outerchr3:43202483..43236664hg18UCSC Ensembl
Outerchr3:43202483..43236664hg17UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg386802
hg196802
hg186802
hg176802
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1672
SamplesNA19240
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)nsv3785
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