A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5606



Internal ID15550432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:170709773..170742839hg38UCSC Ensembl
Outerchr6:171018861..171051927hg19UCSC Ensembl
Outerchr6:170860786..170893852hg18UCSC Ensembl
Outerchr6:170936493..170969559hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg386365
hg196365
hg186365
hg176365
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8332
SamplesNA12156
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)nsv5606
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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