A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8316



Internal ID15188862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:154823438..154868226hg38UCSC Ensembl
Outerchr6:155144572..155189360hg19UCSC Ensembl
Outerchr6:155186264..155231052hg18UCSC Ensembl
Outerchr6:155236685..155281473hg17UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3844789
hg1944789
hg1844789
hg1744789
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5551
Supporting Variants
SamplesNA12156
Known GenesSCAF8
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)nssv8316
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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