A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3932



Internal ID15191973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:20346657..20381885hg38UCSC Ensembl
Outerchr11:20368203..20403431hg19UCSC Ensembl
Outerchr11:20324779..20360007hg18UCSC Ensembl
Outerchr11:20324779..20360007hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg384502
hg194502
hg184502
hg174502
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7702
Supporting Variants
SamplesNA12878
Known GenesHTATIP2
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)nssv3932
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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