A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8249



Internal ID15535615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:51341602..51386552hg38UCSC Ensembl
Outerchr6:51206400..51251350hg19UCSC Ensembl
Outerchr6:51314359..51359309hg18UCSC Ensembl
Outerchr6:51314359..51359309hg17UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg3844951
hg1944951
hg1844951
hg1744951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5302
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)nssv8249
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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