A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1332



Internal ID15197700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:88498027..88515154hg38UCSC Ensembl
Outerchr16:88564435..88581562hg19UCSC Ensembl
Outerchr16:87091936..87109063hg18UCSC Ensembl
Outerchr16:87091936..87109063hg17UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg386083
hg196083
hg186083
hg176083
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1924
Supporting Variants
SamplesNA19240
Known GenesZFPM1
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)nssv1332
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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