A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7735



Internal ID15552774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:35998430..36032536hg38UCSC Ensembl
Outerchr11:36019980..36054086hg19UCSC Ensembl
Outerchr11:35976556..36010662hg18UCSC Ensembl
Outerchr11:35976556..36010662hg17UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg386886
hg196886
hg186886
hg176886
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1002
SamplesNA19240
Known GenesLDLRAD3, MIR3973
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)nsv7735
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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