A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1736



Internal ID15546299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:12383950..12428850hg38UCSC Ensembl
Outerchr16:12477807..12522707hg19UCSC Ensembl
Outerchr16:12385308..12430208hg18UCSC Ensembl
Outerchr16:12385308..12430208hg17UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3844901
hg1944901
hg1844901
hg1744901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7234
SamplesNA12156
Known GenesSNX29
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)nsv1736
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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