A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8216



Internal ID15535648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:6977626..7022326hg38UCSC Ensembl
Outerchr6:6977859..7022559hg19UCSC Ensembl
Outerchr6:6922858..6967558hg18UCSC Ensembl
Outerchr6:6922858..6967558hg17UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3844701
hg1944701
hg1844701
hg1744701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5186
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)nssv8216
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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