A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1463



Internal ID15546026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:23814216..23847085hg38UCSC Ensembl
Outerchr15:24059363..24092232hg19UCSC Ensembl
Outerchr15:21610456..21643325hg18UCSC Ensembl
Outerchr15:21610456..21643325hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg387130
hg197130
hg187130
hg177130
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2102
SamplesNA18555
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)nsv1463
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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