A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8449



Internal ID15535415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:154686158..154720287hg38UCSC Ensembl
Outerchr7:154477868..154511997hg19UCSC Ensembl
Outerchr7:154108801..154142930hg18UCSC Ensembl
Outerchr7:153915516..153949645hg17UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg385305
hg195305
hg185305
hg175305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6016
Supporting Variants
SamplesNA12156
Known GenesDPP6
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)nssv8449
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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