A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8275



Internal ID15535589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:92050684..92095407hg38UCSC Ensembl
Outerchr6:92760402..92805125hg19UCSC Ensembl
Outerchr6:92817123..92861846hg18UCSC Ensembl
Outerchr6:92817123..92861846hg17UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3844724
hg1944724
hg1844724
hg1744724
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5394
Supporting Variants
SamplesNA12156
Known Genes
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)nssv8275
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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