A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1681



Internal ID15546244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:96292909..96305155hg38UCSC Ensembl
Outerchr15:96836138..96848384hg19UCSC Ensembl
Outerchr15:94637142..94649388hg18UCSC Ensembl
Outerchr15:94637142..94649388hg17UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3812247
hg1912247
hg1812247
hg1712247
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7217
SamplesNA12156
Known GenesNR2F2-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)nsv1681
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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