A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10891



Internal ID15539479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:47630891..47644880hg38UCSC Ensembl
Outerchr11:47652443..47666432hg19UCSC Ensembl
Outerchr11:47609019..47623008hg18UCSC Ensembl
Outerchr11:47609019..47623008hg17UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg388485
hg198485
hg188485
hg178485
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv315
Supporting Variants
SamplesNA15510
Known GenesMTCH2
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)nssv10891
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