A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1906



Internal ID15199783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:83630489..83662468hg38UCSC Ensembl
Outerchr16:83664094..83696073hg19UCSC Ensembl
Outerchr16:82221595..82253574hg18UCSC Ensembl
Outerchr16:82221595..82253574hg17UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3831980
hg1931980
hg1831980
hg1731980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9964, nssv1329
SamplesNA18507, NA19240
Known GenesCDH13
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)nsv1906
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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