A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10516



Internal ID15195596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:127237980..127276127hg38UCSC Ensembl
Outerchr6:127559125..127597272hg19UCSC Ensembl
Outerchr6:127600818..127638965hg18UCSC Ensembl
Outerchr6:127600818..127638965hg17UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg3838148
hg1938148
hg1838148
hg1738148
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7385
Supporting Variants
SamplesNA18956
Known GenesRNF146
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)nssv10516
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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