A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6073



Internal ID15537790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:77983163..78029044hg38UCSC Ensembl
Outerchr6:78692880..78738761hg19UCSC Ensembl
Outerchr6:78749599..78795480hg18UCSC Ensembl
Outerchr6:78749599..78795480hg17UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3845882
hg1945882
hg1845882
hg1745882
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5362
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)nssv6073
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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