A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7390



Internal ID15552395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:168655689..168694695hg38UCSC Ensembl
Outerchr6:169056369..169094809hg19UCSC Ensembl
Outerchr6:168798294..168836734hg18UCSC Ensembl
Outerchr6:168874001..168912441hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3839007
hg1938441
hg1838441
hg1738441
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9705
SamplesNA18507
Known GenesSMOC2
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)nsv7390
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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