A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3773



Internal ID15201730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:39868257..39901670hg38UCSC Ensembl
Outerchr3:39909748..39943161hg19UCSC Ensembl
Outerchr3:39884752..39918165hg18UCSC Ensembl
Outerchr3:39884752..39918165hg17UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg386021
hg196021
hg186021
hg176021
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7791
SamplesNA12156
Known GenesMYRIP
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)nsv3773
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