A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1545



Internal ID15199422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:56367300..56605183hg38UCSC Ensembl
Outerchr15:56659498..56897381hg19UCSC Ensembl
Outerchr15:54446790..54684673hg18UCSC Ensembl
Outerchr15:54446790..54684673hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38237884
hg19237884
hg18237884
hg17237884
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6634, nssv9516
SamplesNA18507, NA12156
Known GenesMNS1, TEX9
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)nsv1545
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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