A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9686



Internal ID15193431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:24773921..24823784hg38UCSC Ensembl
Outerchr6:24774149..24824012hg19UCSC Ensembl
Outerchr6:24882128..24931991hg18UCSC Ensembl
Outerchr6:24882128..24931991hg17UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3849864
hg1949864
hg1849864
hg1749864
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5227
Supporting Variants
SamplesNA18507
Known GenesFAM65B, GMNN, LOC101928603
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)nssv9686
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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