A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1530



Internal ID15199407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:50010327..50055419hg38UCSC Ensembl
Outerchr15:50302524..50347616hg19UCSC Ensembl
Outerchr15:48089816..48134908hg18UCSC Ensembl
Outerchr15:48089816..48134908hg17UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3845093
hg1945093
hg1845093
hg1745093
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7168
SamplesNA12156
Known GenesATP8B4
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)nsv1530
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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