A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7388



Internal ID15552392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:166471931..166511856hg38UCSC Ensembl
Outerchr6:166885419..166925344hg19UCSC Ensembl
Outerchr6:166805409..166845334hg18UCSC Ensembl
Outerchr6:166855830..166895755hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3839926
hg1939926
hg1839926
hg1739926
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv602
SamplesNA19240
Known GenesMIR1913, RPS6KA2
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)nsv7388
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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