A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1496



Internal ID15199373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:37012976..37057466hg38UCSC Ensembl
Outerchr15:37305177..37349667hg19UCSC Ensembl
Outerchr15:35092469..35136959hg18UCSC Ensembl
Outerchr15:35092469..35136959hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3844491
hg1944491
hg1844491
hg1744491
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4145
SamplesNA12878
Known GenesMEIS2
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)nsv1496
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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