A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1562



Internal ID15199439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:62819554..62854951hg38UCSC Ensembl
Outerchr15:63111753..63147150hg19UCSC Ensembl
Outerchr15:60898806..60934203hg18UCSC Ensembl
Outerchr15:60898806..60934203hg17UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg384340
hg194340
hg184340
hg174340
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4156
SamplesNA12878
Known GenesMIR190A, TLN2
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)nsv1562
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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