A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1490



Internal ID15546053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:35722024..35755362hg38UCSC Ensembl
Outerchr15:36014225..36047563hg19UCSC Ensembl
Outerchr15:33801517..33834855hg18UCSC Ensembl
Outerchr15:33801517..33834855hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3833339
hg1933339
hg1833339
hg1733339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7156
SamplesNA12156
Known GenesDPH6-AS1
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)nsv1490
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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