A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3904



Internal ID15548560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:87682594..87716229hg38UCSC Ensembl
Outerchr3:87731744..87765379hg19UCSC Ensembl
Outerchr3:87814434..87848069hg18UCSC Ensembl
Outerchr3:87814434..87848069hg17UCSC Ensembl
Cytoband3p11.2
Allele length
AssemblyAllele length
hg386384
hg196384
hg186384
hg176384
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3103
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)nsv3904
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