A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7213



Internal ID15205514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1879030..1978829hg38UCSC Ensembl
Outerchr11:1900260..2000059hg19UCSC Ensembl
Outerchr11:1856836..1956635hg18UCSC Ensembl
Outerchr11:1856836..1956635hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3899800
hg1999800
hg1899800
hg1799800
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9813, nssv984, nssv10793, nssv6437, nssv5339, nssv6436, nssv982, nssv5341, nssv10884, nssv3917, nssv9266, nssv10792, nssv1921, nssv1922
SamplesNA18507, NA12156, NA12878, NA18956, NA15510, NA18555, NA18517, NA19240, NA19129
Known GenesLSP1, MRPL23, TNNT3
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)nsv7213
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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