A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11130



Internal ID15539449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:98474584..98504004hg38UCSC Ensembl
Outerchr6:98922460..98951880hg19UCSC Ensembl
Outerchr6:99029181..99058601hg18UCSC Ensembl
Outerchr6:99029181..99058601hg17UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3810467
hg1910467
hg1810467
hg1710467
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5406
Supporting Variants
SamplesNA15510
Known Genes
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)nssv11130
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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