A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1528



Internal ID15546091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:49775761..49820761hg38UCSC Ensembl
Outerchr15:50067958..50112958hg19UCSC Ensembl
Outerchr15:47855250..47900250hg18UCSC Ensembl
Outerchr15:47855250..47900250hg17UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3845001
hg1945001
hg1845001
hg1745001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7167
SamplesNA12156
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)nsv1528
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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