A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7640



Internal ID15205984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1517222..1553683hg38UCSC Ensembl
Outerchr11:1538452..1574913hg19UCSC Ensembl
Outerchr11:1495028..1531489hg18UCSC Ensembl
Outerchr11:1495028..1531489hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg387961
hg197961
hg187961
hg177961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3915, nssv6434, nssv10791, nssv5337, nssv1919, nssv9939
SamplesNA18507, NA12156, NA12878, NA18956, NA18555, NA19129
Known GenesMOB2
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)nsv7640
Frequency
Sample Size9
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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