A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7733



Internal ID15206086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:35243420..35276063hg38UCSC Ensembl
Outerchr11:35264967..35297610hg19UCSC Ensembl
Outerchr11:35221543..35254186hg18UCSC Ensembl
Outerchr11:35221543..35254186hg17UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg386848
hg196848
hg186848
hg176848
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10814
SamplesNA18956
Known GenesSLC1A2
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)nsv7733
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