A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5013



Internal ID15543257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:106325308..106335029hg38UCSC Ensembl
Outerchr7:105965754..105975475hg19UCSC Ensembl
Outerchr7:105752990..105762711hg18UCSC Ensembl
Outerchr7:105559705..105569426hg17UCSC Ensembl
Cytoband7q22.2
Allele length
AssemblyAllele length
hg386154
hg196154
hg186154
hg176154
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5892
Supporting Variants
SamplesNA19129
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)nssv5013
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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