A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1737



Internal ID15199614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:12922406..12967034hg38UCSC Ensembl
Outerchr16:13016263..13060891hg19UCSC Ensembl
Outerchr16:12923764..12968392hg18UCSC Ensembl
Outerchr16:12923764..12968392hg17UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3844629
hg1944629
hg1844629
hg1744629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4640
SamplesNA19129
Known GenesSHISA9
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)nsv1737
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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