A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1493



Internal ID15546056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:36417393..36449852hg38UCSC Ensembl
Outerchr15:36709594..36742053hg19UCSC Ensembl
Outerchr15:34496886..34529345hg18UCSC Ensembl
Outerchr15:34496886..34529345hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg387566
hg197566
hg187566
hg177566
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2107
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)nsv1493
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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