A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3926



Internal ID15538653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:9582875..9615821hg38UCSC Ensembl
Outerchr11:9604422..9637368hg19UCSC Ensembl
Outerchr11:9560998..9593944hg18UCSC Ensembl
Outerchr11:9560998..9593944hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg386800
hg196800
hg186800
hg176800
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7672
Supporting Variants
SamplesNA12878
Known GenesWEE1
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)nssv3926
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