A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8361



Internal ID15188817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:35681099..35714230hg38UCSC Ensembl
Outerchr7:35720709..35753840hg19UCSC Ensembl
Outerchr7:35687234..35720365hg18UCSC Ensembl
Outerchr7:35493949..35527080hg17UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg386308
hg196308
hg186308
hg176308
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5699
Supporting Variants
SamplesNA12156
Known GenesHERPUD2
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)nssv8361
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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