A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11061



Internal ID15539647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:55845935..55861081hg38UCSC Ensembl
Outerchr3:55879963..55895109hg19UCSC Ensembl
Outerchr3:55855003..55870149hg18UCSC Ensembl
Outerchr3:55855003..55870149hg17UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg388704
hg198704
hg188704
hg178704
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3833
Supporting Variants
SamplesNA15510
Known GenesERC2, MIR3938
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)nssv11061
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