A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv977



Internal ID15198254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:274155..315831hg38UCSC Ensembl
Outerchr11:274155..315831hg19UCSC Ensembl
Outerchr11:264155..305831hg18UCSC Ensembl
Outerchr11:264155..305831hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3841677
hg1941677
hg1841677
hg1741677
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7212
Supporting Variants
SamplesNA19240
Known GenesATHL1, IFITM1, IFITM2, IFITM5, NLRP6
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)nssv977
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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