A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6661



Internal ID15537202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:18799187..18835384hg38UCSC Ensembl
Outerchr16:18810509..18846706hg19UCSC Ensembl
Outerchr16:18718010..18754207hg18UCSC Ensembl
Outerchr16:18718010..18754207hg17UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3836198
hg1936198
hg1836198
hg1736198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1752
Supporting Variants
SamplesNA12156
Known GenesARL6IP1, SMG1
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)nssv6661
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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