A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1831



Internal ID15546394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:65038073..65072202hg38UCSC Ensembl
Outerchr16:65071976..65106105hg19UCSC Ensembl
Outerchr16:63629477..63663606hg18UCSC Ensembl
Outerchr16:63629477..63663606hg17UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3834130
hg1934130
hg1834130
hg1734130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2145
SamplesNA18555
Known GenesCDH11
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)nsv1831
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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