A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1486



Internal ID15199363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:35202047..35244348hg38UCSC Ensembl
Outerchr15:35494248..35536549hg19UCSC Ensembl
Outerchr15:33281540..33323841hg18UCSC Ensembl
Outerchr15:33281540..33323841hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3842302
hg1942302
hg1842302
hg1742302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6626
SamplesNA12156
Known GenesANP32AP1
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)nsv1486
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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