A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11121



Internal ID15539458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:23243244..23272712hg38UCSC Ensembl
Outerchr6:23243472..23272940hg19UCSC Ensembl
Outerchr6:23351451..23380919hg18UCSC Ensembl
Outerchr6:23351451..23380919hg17UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3810403
hg1910403
hg1810403
hg1710403
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5225
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)nssv11121
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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