A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7637



Internal ID15205980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:996222..1029656hg38UCSC Ensembl
Outerchr11:996222..1029656hg19UCSC Ensembl
Outerchr11:986222..1019656hg18UCSC Ensembl
Outerchr11:986222..1019656hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg388826
hg198826
hg188826
hg178826
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5335, nssv1917, nssv10789, nssv3913, nssv6431, nssv978, nssv11246, nssv9937
SamplesNA18507, NA15510, NA18956, NA19129, NA12156, NA12878, NA19240, NA18555
Known GenesAP2A2, MUC6
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)nsv7637
Frequency
Sample Size9
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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