A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7752



Internal ID15552793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:43094461..43125926hg38UCSC Ensembl
Outerchr11:43116011..43147476hg19UCSC Ensembl
Outerchr11:43072587..43104052hg18UCSC Ensembl
Outerchr11:43072587..43104052hg17UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg388032
hg198032
hg188032
hg178032
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10815
SamplesNA18956
Known Genes
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)nsv7752
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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