A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6058



Internal ID15191120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:26688691..26774936hg19UCSC Ensembl
Outerchr6:26796670..26882915hg18UCSC Ensembl
Outerchr6:26796670..26882915hg17UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg1986246
hg1886246
hg1786246
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7378
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)nssv6058
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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