A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1511



Internal ID8513056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:43021641..43053576hg38UCSC Ensembl
Outerchr15:43313839..43345774hg19UCSC Ensembl
Outerchr15:41101131..41133066hg18UCSC Ensembl
Outerchr15:41101131..41133066hg17UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg387562
hg197562
hg187562
hg177562
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10047
SamplesNA18956
Known GenesUBR1
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)nsv1511
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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