A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1523



Internal ID15546086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:45457702..45491627hg38UCSC Ensembl
Outerchr15:45749900..45783825hg19UCSC Ensembl
Outerchr15:43537192..43571117hg18UCSC Ensembl
Outerchr15:43537192..43571117hg17UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3833926
hg1933926
hg1833926
hg1733926
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7164
SamplesNA12156
Known GenesSLC30A4
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)nsv1523
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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