A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7222



Internal ID15552210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:89811778..90079788hg38UCSC Ensembl
Outerchr11:89544946..89812956hg19UCSC Ensembl
Outerchr11:89184594..89452604hg18UCSC Ensembl
Outerchr11:89184594..89452604hg17UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38268011
hg19268011
hg18268011
hg17268011
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6472, nssv3976, nssv9273, nssv6473, nssv1948, nssv1949, nssv3975, nssv1026
SamplesNA12156, NA12878, NA18555, NA18517, NA19240
Known GenesMIR5692A1, TRIM49C, TRIM49D1, TRIM49D2P, TRIM53AP, TRIM64, TRIM64B
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)nsv7222
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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