A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4097



Internal ID15548772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:163698847..163722463hg38UCSC Ensembl
Outerchr3:163416635..163440251hg19UCSC Ensembl
Outerchr3:164899329..164922945hg18UCSC Ensembl
Outerchr3:164899337..164922953hg17UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg387706
hg197706
hg187706
hg177706
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10373
SamplesNA18956
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)nsv4097
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