A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8414



Internal ID15535450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:105934576..105977392hg38UCSC Ensembl
Outerchr7:105575022..105617838hg19UCSC Ensembl
Outerchr7:105362258..105405074hg18UCSC Ensembl
Outerchr7:105168973..105211789hg17UCSC Ensembl
Cytoband7q22.2
Allele length
AssemblyAllele length
hg3842817
hg1942817
hg1842817
hg1742817
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5891
Supporting Variants
SamplesNA12156
Known GenesCDHR3
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)nssv8414
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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