A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1315



Internal ID15544404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:69968612..70234953hg38UCSC Ensembl
Outerchr16:70002515..70268856hg19UCSC Ensembl
Outerchr16:68560016..68826357hg18UCSC Ensembl
Outerchr16:68560016..68826357hg17UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38266342
hg19266342
hg18266342
hg17266342
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1853
Supporting Variants
SamplesNA19240
Known GenesCLEC18C, LOC100506060, MIR1972-1, MIR1972-2, PDPR, PDXDC2P
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)nssv1315
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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