A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1645



Internal ID15546208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:85028984..85047864hg38UCSC Ensembl
Outerchr15:85572215..85591095hg19UCSC Ensembl
Outerchr15:83373219..83392099hg18UCSC Ensembl
Outerchr15:83373219..83392099hg17UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3818881
hg1918881
hg1818881
hg1718881
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7209
SamplesNA12156
Known GenesPDE8A
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)nsv1645
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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