A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7739



Internal ID15552778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:38189170..38220912hg38UCSC Ensembl
Outerchr11:38210720..38242462hg19UCSC Ensembl
Outerchr11:38167296..38199038hg18UCSC Ensembl
Outerchr11:38167296..38199038hg17UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg387544
hg197544
hg187544
hg177544
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5355
SamplesNA19129
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)nsv7739
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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