A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8314



Internal ID15535550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:150018561..150040523hg38UCSC Ensembl
Outerchr6:150339697..150361659hg19UCSC Ensembl
Outerchr6:150381390..150403352hg18UCSC Ensembl
Outerchr6:150431811..150453773hg17UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3821963
hg1921963
hg1821963
hg1721963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5535
Supporting Variants
SamplesNA12156
Known GenesRAET1L
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)nssv8314
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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