A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1020



Internal ID15198042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:72270271..72304844hg38UCSC Ensembl
Outerchr11:71981315..72015888hg19UCSC Ensembl
Outerchr11:71658963..71693536hg18UCSC Ensembl
Outerchr11:71658963..71693536hg17UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg386425
hg196425
hg186425
hg176425
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv385
Supporting Variants
SamplesNA19240
Known GenesCLPB
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)nssv1020
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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