A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2857



Internal ID15195018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:9016127..9050514hg38UCSC Ensembl
Outerchr11:9037674..9072061hg19UCSC Ensembl
Outerchr11:8994250..9028637hg18UCSC Ensembl
Outerchr11:8994250..9028637hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg385610
hg195610
hg185610
hg175610
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7667
Supporting Variants
SamplesNA18555
Known GenesSCUBE2
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)nssv2857
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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